ENST00000350026.11:c.3808A>G
|
ENSP00000055163.8:p.Ser1270Gly
|
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ENST00000414678.8:c.3877A>G
|
ENSP00000412835.3:p.Ser1293Gly
|
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ENST00000637015.2:c.4096A>G
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ENSP00000489729.2:p.Ser1366Gly
|
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ENST00000346085.10:c.3847A>G
|
ENSP00000344546.5:p.Ser1283Gly
|
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ENST00000350026.10:c.3559A>G
|
ENSP00000055163.7:p.Ser1187Gly
|
|
ENST00000414678.7:c.2125A>G
|
ENSP00000412835.2:p.Ser709Gly
|
|
ENST00000635849.1:c.1288A>G
|
ENSP00000490948.1:p.Ser430Gly
|
|
ENST00000635957.1:c.922A>G
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ENSP00000490385.1:p.Ser308Gly
|
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ENST00000636930.2:c.3967A>G
MANE Select
|
ENSP00000490491.2:p.Ser1323Gly
|
|
ENST00000636940.1:n.1964A>G
|
|
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ENST00000637015.1:c.1335A>G
|
|
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ENST00000637568.1:c.1249A>G
|
|
|
ENST00000637741.1:n.633A>G
|
|
|
ENST00000637810.1:c.1309A>G
|
ENSP00000489636.1:p.Ser437Gly
|
|
ENST00000637904.1:c.1468A>G
|
ENSP00000490550.1:p.Ser490Gly
|
|
ENST00000647938.1:c.3598A>G
|
ENSP00000498155.1:p.Ser1200Gly
|
|
ENST00000346085.9:c.3598A>G
|
ENSP00000344546.4:p.Ser1200Gly
|
|
ENST00000350026.9:c.3559A>G
|
ENSP00000055163.7:p.Ser1187Gly
|
|
ENST00000414678.6:c.2125A>G
|
ENSP00000412835.2:p.Ser709Gly
|
|
NM_017519.2:c.3559A>G
|
NP_059989.2:p.Ser1187Gly
|
|
NM_020732.3:c.3598A>G
|
NP_065783.3:p.Ser1200Gly
|
|
XM_005267069.3:c.3718A>G
|
XP_005267126.2:p.Ser1240Gly
|
|
XM_011535984.1:c.2797A>G
|
XP_011534286.1:p.Ser933Gly
|
|
XM_011535985.1:c.2617A>G
|
XP_011534287.1:p.Ser873Gly
|
|
XM_011535986.1:c.2377A>G
|
XP_011534288.1:p.Ser793Gly
|
|
XM_011535987.1:c.1996A>G
|
XP_011534289.1:p.Ser666Gly
|
|
XM_011535988.1:c.859A>G
|
XP_011534290.1:p.Ser287Gly
|
|
NM_001346813.1:c.3718A>G
|
NP_001333742.1:p.Ser1240Gly
|
|
NM_001363725.1:c.1468A>G
|
NP_001350654.1:p.Ser490Gly
|
|
XM_011535984.2:c.3928A>G
|
XP_011534286.2:p.Ser1310Gly
|
|
XM_011535988.3:c.859A>G
|
XP_011534290.1:p.Ser287Gly
|
|
XM_017011103.2:c.3829A>G
|
XP_016866592.1:p.Ser1277Gly
|
|
XM_017011104.1:c.3799A>G
|
XP_016866593.1:p.Ser1267Gly
|
|
XM_017011105.2:c.3769A>G
|
XP_016866594.1:p.Ser1257Gly
|
|
XM_017011106.2:c.3640A>G
|
XP_016866595.1:p.Ser1214Gly
|
|
XM_017011107.2:c.3619A>G
|
XP_016866596.1:p.Ser1207Gly
|
|
XR_002956289.1:n.4011A>G
|
|
|
NM_001363725.2:c.1468A>G
|
NP_001350654.1:p.Ser490Gly
|
|
NM_001371656.1:c.3847A>G
|
NP_001358585.1:p.Ser1283Gly
|
|
NM_001374820.1:c.3847A>G
|
NP_001361749.1:p.Ser1283Gly
|
|
NM_001374828.1:c.3967A>G
MANE Select
|
NP_001361757.1:p.Ser1323Gly
|
|
NM_017519.3:c.3808A>G
|
NP_059989.3:p.Ser1270Gly
|
|