ENST00000401669.7:c.3777T>C
MANE Select
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ENSP00000385017.2:p.Gly1259=
|
|
ENST00000637889.1:n.944T>C
|
|
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ENST00000637906.1:c.606-1396T>C
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ENSP00000490198.1:n.606-1396T>C
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|
ENST00000342183.9:c.614-1396T>C
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ENSP00000341184.5:n.614-1396T>C
|
|
ENST00000401669.6:c.3777T>C
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ENSP00000385017.2:p.Gly1259=
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|
ENST00000401710.5:c.672T>C
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ENSP00000385580.2:p.Gly224=
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|
ENST00000404971.5:c.3897T>C
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ENSP00000385142.1:p.Gly1299=
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ENST00000405472.7:c.3741T>C
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ENSP00000434015.2:p.Gly1247=
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|
ENST00000406316.6:c.3719-1396T>C
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ENSP00000384311.2:n.3719-1396T>C
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ENST00000611589.4:c.-119-1396T>C
|
ENSP00000483634.1:n.-119-1396T>C
|
|
ENST00000625672.2:c.3753T>C
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ENSP00000485887.1:p.Gly1251=
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ENST00000628364.2:c.672T>C
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ENSP00000485815.1:p.Gly224=
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ENST00000630543.2:c.3753T>C
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ENSP00000486879.1:p.Gly1251=
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ENST00000635264.1:n.586T>C
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|
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NM_001135659.1:c.3897T>C
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NP_001129131.1:p.Gly1299=
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NM_004801.4:c.3719-1396T>C
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NP_004792.1:n.3719-1396T>C
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NM_138735.2:c.614-1396T>C
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NP_620072.1:n.614-1396T>C
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XM_005264642.2:c.3798T>C
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XP_005264699.1:p.Gly1266=
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XM_005264643.2:c.3753T>C
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XP_005264700.1:p.Gly1251=
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XM_006712137.2:c.3740-1396T>C
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XP_006712200.1:n.3740-1396T>C
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XM_006712140.2:c.3798T>C
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XP_006712203.1:p.Gly1266=
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XM_011533167.1:c.3798T>C
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XP_011531469.1:p.Gly1266=
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XM_011533168.1:c.3795T>C
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XP_011531470.1:p.Gly1265=
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XM_011533169.1:c.3786T>C
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XP_011531471.1:p.Gly1262=
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XM_011533170.1:c.3780T>C
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XP_011531472.1:p.Gly1260=
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XM_011533171.1:c.3777T>C
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XP_011531473.1:p.Gly1259=
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XM_011533172.1:c.3771T>C
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XP_011531474.1:p.Gly1257=
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XM_011533173.1:c.3768T>C
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XP_011531475.1:p.Gly1256=
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XM_011533174.1:c.3753T>C
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XP_011531476.1:p.Gly1251=
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XM_011533175.1:c.3741T>C
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XP_011531477.1:p.Gly1247=
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XM_011533176.1:c.3738T>C
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XP_011531478.1:p.Gly1246=
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XM_011533177.1:c.3740-1396T>C
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XP_011531479.1:n.3740-1396T>C
|
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XM_011533178.1:c.3708T>C
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XP_011531480.1:p.Gly1236=
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XM_011533179.1:c.3695-1396T>C
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XP_011531481.1:n.3695-1396T>C
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XM_011533180.1:c.3798T>C
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XP_011531482.1:p.Gly1266=
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XM_011533181.1:c.3003T>C
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XP_011531483.1:p.Gly1001=
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XM_011533182.1:c.2958T>C
|
XP_011531484.1:p.Gly986=
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|
XM_011533183.1:c.2931T>C
|
XP_011531485.1:p.Gly977=
|
|
XM_011533184.1:c.2838T>C
|
XP_011531486.1:p.Gly946=
|
|
NM_001135659.2:c.3897T>C
|
NP_001129131.1:p.Gly1299=
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|
NM_001330077.1:c.3753T>C
|
NP_001317006.1:p.Gly1251=
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|
NM_001330078.1:c.3777T>C
|
NP_001317007.1:p.Gly1259=
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|
NM_001330082.1:c.3753T>C
|
NP_001317011.1:p.Gly1251=
|
|
NM_001330083.1:c.3653-1396T>C
|
NP_001317012.1:n.3653-1396T>C
|
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NM_001330084.1:c.3711T>C
|
NP_001317013.1:p.Gly1237=
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|
NM_001330085.1:c.3750T>C
|
NP_001317014.1:p.Gly1250=
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|
NM_001330086.1:c.3777T>C
|
NP_001317015.1:p.Gly1259=
|
|
NM_001330087.1:c.3608-1396T>C
|
NP_001317016.1:n.3608-1396T>C
|
|
NM_001330088.1:c.3638-1396T>C
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NP_001317017.1:n.3638-1396T>C
|
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NM_001330091.1:c.672T>C
|
NP_001317020.1:p.Gly224=
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|
NM_001330092.1:c.672T>C
|
NP_001317021.1:p.Gly224=
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|
NM_001330093.1:c.3774T>C
|
NP_001317022.1:p.Gly1258=
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|
NM_001330094.1:c.3765T>C
|
NP_001317023.1:p.Gly1255=
|
|
NM_001330095.1:c.3668-1396T>C
|
NP_001317024.1:n.3668-1396T>C
|
|
NM_001330096.1:c.3608-1396T>C
|
NP_001317025.1:n.3608-1396T>C
|
|
NM_001330097.1:c.614-1396T>C
|
NP_001317026.1:n.614-1396T>C
|
|
NM_004801.5:c.3719-1396T>C
|
NP_004792.1:n.3719-1396T>C
|
|
NM_138735.4:c.614-1396T>C
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NP_620072.1:n.614-1396T>C
|
|
XM_005264642.4:c.3798T>C
|
XP_005264699.1:p.Gly1266=
|
|
XM_006712137.4:c.3740-1396T>C
|
XP_006712200.1:n.3740-1396T>C
|
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XM_006712140.4:c.3825T>C
|
XP_006712203.2:p.Gly1275=
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XM_011533167.3:c.3798T>C
|
XP_011531469.1:p.Gly1266=
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|
XM_011533172.3:c.3771T>C
|
XP_011531474.1:p.Gly1257=
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|
XM_011533175.3:c.3741T>C
|
XP_011531477.1:p.Gly1247=
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|
XM_011533177.3:c.3740-1396T>C
|
XP_011531479.1:n.3740-1396T>C
|
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XM_011533178.3:c.3708T>C
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XP_011531480.1:p.Gly1236=
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XM_011533180.3:c.3798T>C
|
XP_011531482.1:p.Gly1266=
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|
XM_011533183.2:c.2931T>C
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XP_011531485.1:p.Gly977=
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|
XM_017005303.2:c.3825T>C
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XP_016860792.1:p.Gly1275=
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XM_017005304.2:c.3822T>C
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XP_016860793.1:p.Gly1274=
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|
XM_017005305.2:c.3825T>C
|
XP_016860794.1:p.Gly1275=
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|
XM_017005306.2:c.3813T>C
|
XP_016860795.1:p.Gly1271=
|
|
XM_017005307.2:c.3807T>C
|
XP_016860796.1:p.Gly1269=
|
|
XM_017005308.2:c.3804T>C
|
XP_016860797.1:p.Gly1268=
|
|
XM_017005309.2:c.3798T>C
|
XP_016860798.1:p.Gly1266=
|
|
XM_017005310.2:c.3795T>C
|
XP_016860799.1:p.Gly1265=
|
|
XM_017005311.2:c.3780T>C
|
XP_016860800.1:p.Gly1260=
|
|
XM_017005314.2:c.3765T>C
|
XP_016860803.1:p.Gly1255=
|
|
XM_017005315.2:c.3771T>C
|
XP_016860804.1:p.Gly1257=
|
|
XM_017005316.2:c.3762T>C
|
XP_016860805.1:p.Gly1254=
|
|
XM_017005318.2:c.3753T>C
|
XP_016860807.1:p.Gly1251=
|
|
XM_017005320.2:c.3750T>C
|
XP_016860809.1:p.Gly1250=
|
|
XM_017005321.2:c.3767-1396T>C
|
XP_016860810.1:n.3767-1396T>C
|
|
XM_017005322.2:c.3767-1396T>C
|
XP_016860811.1:n.3767-1396T>C
|
|
XM_017005324.2:c.3713-1396T>C
|
XP_016860813.1:n.3713-1396T>C
|
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XM_017005325.2:c.3713-1396T>C
|
XP_016860814.1:n.3713-1396T>C
|
|
XM_017005326.2:c.3701-1396T>C
|
XP_016860815.1:n.3701-1396T>C
|
|
XM_017005327.2:c.3695-1396T>C
|
XP_016860816.1:n.3695-1396T>C
|
|
XM_017005329.2:c.3825T>C
|
XP_016860818.1:p.Gly1275=
|
|
XM_017005334.2:c.2865T>C
|
XP_016860823.1:p.Gly955=
|
|
NM_001330078.2:c.3777T>C
MANE Select
|
NP_001317007.1:p.Gly1259=
|
|
NM_001135659.3:c.3897T>C
|
NP_001129131.1:p.Gly1299=
|
|
NM_001330077.2:c.3753T>C
|
NP_001317006.1:p.Gly1251=
|
|
NM_001330082.2:c.3753T>C
|
NP_001317011.1:p.Gly1251=
|
|
NM_001330083.2:c.3653-1396T>C
|
NP_001317012.1:n.3653-1396T>C
|
|
NM_001330084.2:c.3711T>C
|
NP_001317013.1:p.Gly1237=
|
|
NM_001330085.2:c.3750T>C
|
NP_001317014.1:p.Gly1250=
|
|
NM_001330086.2:c.3777T>C
|
NP_001317015.1:p.Gly1259=
|
|
NM_001330087.2:c.3608-1396T>C
|
NP_001317016.1:n.3608-1396T>C
|
|
NM_001330088.2:c.3638-1396T>C
|
NP_001317017.1:n.3638-1396T>C
|
|
NM_001330091.2:c.672T>C
|
NP_001317020.1:p.Gly224=
|
|
NM_001330092.2:c.672T>C
|
NP_001317021.1:p.Gly224=
|
|
NM_001330093.2:c.3774T>C
|
NP_001317022.1:p.Gly1258=
|
|
NM_001330094.2:c.3765T>C
|
NP_001317023.1:p.Gly1255=
|
|
NM_001330095.2:c.3668-1396T>C
|
NP_001317024.1:n.3668-1396T>C
|
|
NM_001330096.2:c.3608-1396T>C
|
NP_001317025.1:n.3608-1396T>C
|
|
NM_001330097.2:c.614-1396T>C
|
NP_001317026.1:n.614-1396T>C
|
|
NM_004801.6:c.3719-1396T>C
|
NP_004792.1:n.3719-1396T>C
|
|
NM_138735.5:c.614-1396T>C
|
NP_620072.1:n.614-1396T>C
|
|