ENST00000378154.3:c.2447C>G
|
ENSP00000367396.2:p.Ala816Gly
|
|
ENST00000378158.6:c.2444C>G
|
ENSP00000367400.2:p.Ala815Gly
|
|
ENST00000378163.7:c.2498C>G
MANE Select
|
ENSP00000367405.1:p.Ala833Gly
|
|
ENST00000378166.9:c.2396C>G
|
ENSP00000367408.5:p.Ala799Gly
|
|
ENST00000378168.8:c.2501C>G
|
ENSP00000367410.4:p.Ala834Gly
|
|
ENST00000378179.9:c.1118C>G
|
ENSP00000367421.4:p.Ala373Gly
|
|
ENST00000421587.8:c.2429C>G
|
ENSP00000400526.4:p.Ala810Gly
|
|
ENST00000442742.7:c.2360C>G
|
ENSP00000398007.3:p.Ala787Gly
|
|
ENST00000642499.1:n.1277C>G
|
|
|
ENST00000643733.1:c.270C>G
|
|
|
ENST00000644219.1:c.2480C>G
|
ENSP00000495357.1:p.Ala827Gly
|
|
ENST00000644347.1:c.2411C>G
|
ENSP00000494183.1:p.Ala804Gly
|
|
ENST00000645566.1:c.2483C>G
|
ENSP00000494788.1:p.Ala828Gly
|
|
ENST00000645937.2:n.2729C>G
|
|
|
ENST00000645986.2:c.2465C>G
|
ENSP00000494409.2:p.Ala822Gly
|
|
ENST00000646087.2:c.1820C>G
|
ENSP00000495510.2:p.Ala607Gly
|
|
ENST00000646120.2:c.2414C>G
|
ENSP00000495291.2:p.Ala805Gly
|
|
ENST00000675354.1:c.2432C>G
|
ENSP00000502315.1:p.Ala811Gly
|
|
ENST00000378158.5:c.2447C>G
|
ENSP00000367400.1:p.Ala816Gly
|
|
ENST00000378163.5:c.2498C>G
|
ENSP00000367405.1:p.Ala833Gly
|
|
ENST00000378166.8:c.2483C>G
|
ENSP00000367408.4:p.Ala828Gly
|
|
ENST00000378168.6:c.863C>G
|
ENSP00000367410.2:p.Ala288Gly
|
|
ENST00000378179.7:c.1274C>G
|
ENSP00000367421.3:p.Ala425Gly
|
|
ENST00000421587.6:c.2411C>G
|
ENSP00000400526.2:p.Ala804Gly
|
|
ENST00000442742.6:c.2414C>G
|
ENSP00000398007.2:p.Ala805Gly
|
|
NM_001126054.2:c.2414C>G
|
NP_001119526.1:p.Ala805Gly
|
|
NM_001126055.2:c.2411C>G
|
NP_001119527.1:p.Ala804Gly
|
|
NM_003688.3:c.2483C>G
|
NP_003679.2:p.Ala828Gly
|
|
XM_005272686.3:c.2480C>G
|
XP_005272743.1:p.Ala827Gly
|
|
XM_006724566.2:c.2375C>G
|
XP_006724629.1:p.Ala792Gly
|
|
XM_011543993.1:c.2498C>G
|
XP_011542295.1:p.Ala833Gly
|
|
XM_011543994.1:c.2462C>G
|
XP_011542296.1:p.Ala821Gly
|
|
XM_011543995.1:c.2429C>G
|
XP_011542297.1:p.Ala810Gly
|
|
XM_011543996.1:c.2393C>G
|
XP_011542298.1:p.Ala798Gly
|
|
XM_011543997.1:c.1925C>G
|
XP_011542299.1:p.Ala642Gly
|
|
XM_005272686.4:c.2480C>G
|
XP_005272743.1:p.Ala827Gly
|
|
XM_006724566.3:c.2375C>G
|
XP_006724629.1:p.Ala792Gly
|
|
XM_011543993.2:c.2498C>G
|
XP_011542295.1:p.Ala833Gly
|
|
XM_011543994.2:c.2462C>G
|
XP_011542296.1:p.Ala821Gly
|
|
XM_011543995.2:c.2429C>G
|
XP_011542297.1:p.Ala810Gly
|
|
XM_011543996.2:c.2393C>G
|
XP_011542298.1:p.Ala798Gly
|
|
XM_011543997.3:c.1925C>G
|
XP_011542299.1:p.Ala642Gly
|
|
XM_024452473.1:c.1820C>G
|
XP_024308241.1:p.Ala607Gly
|
|
NM_001367721.1:c.2498C>G
MANE Select
|
NP_001354650.1:p.Ala833Gly
|
|