ENST00000706271.1:c.488C>T
|
ENSP00000516315.1:p.Ala163Val
|
|
ENST00000706272.1:c.571C>T
|
|
|
ENST00000304623.13:c.1499C>T
MANE Select
|
ENSP00000307134.8:p.Ala500Val
|
|
ENST00000304623.12:c.1499C>T
|
ENSP00000307134.8:p.Ala500Val
|
|
ENST00000495388.6:n.584C>T
|
|
|
ENST00000503622.5:c.488C>T
|
ENSP00000426887.1:p.Ala163Val
|
|
ENST00000504354.5:n.538C>T
|
|
|
ENST00000504499.5:c.*238C>T
|
ENSP00000421000.1:n.*238C>T
|
|
ENST00000511377.5:c.1226C>T
|
ENSP00000426510.1:p.Ala409Val
|
|
ENST00000513588.5:c.761C>T
|
ENSP00000421093.1:p.Ala254Val
|
|
NM_001288715.1:c.1226C>T
|
NP_001275644.1:p.Ala409Val
|
|
NM_001288716.1:c.488C>T
|
NP_001275645.1:p.Ala163Val
|
|
NM_001288717.1:c.200C>T
|
NP_001275646.1:p.Ala67Val
|
|
NM_001332.3:c.1499C>T
|
NP_001323.1:p.Ala500Val
|
|
NR_109988.1:n.951C>T
|
|
|
XM_005248251.2:c.1499C>T
|
XP_005248308.1:p.Ala500Val
|
|
XM_005248252.1:c.1457C>T
|
XP_005248309.1:p.Ala486Val
|
|
XM_005248253.1:c.1226C>T
|
XP_005248310.1:p.Ala409Val
|
|
XM_011513967.1:c.1226C>T
|
XP_011512269.1:p.Ala409Val
|
|
NM_001364128.1:c.488C>T
|
NP_001351057.1:p.Ala163Val
|
|
XM_005248251.3:c.1499C>T
|
XP_005248308.1:p.Ala500Val
|
|
XM_005248252.2:c.1457C>T
|
XP_005248309.1:p.Ala486Val
|
|
XM_011513967.2:c.1226C>T
|
XP_011512269.1:p.Ala409Val
|
|
XM_017009072.1:c.761C>T
|
XP_016864561.1:p.Ala254Val
|
|
XM_017009073.1:c.719C>T
|
XP_016864562.1:p.Ala240Val
|
|
XM_017009074.1:c.761C>T
|
XP_016864563.1:p.Ala254Val
|
|
XM_017009075.2:c.488C>T
|
XP_016864564.1:p.Ala163Val
|
|
XM_024454368.1:c.-44+18195C>T
|
XP_024310136.1:n.-44+18195C>T
|
|
NM_001332.4:c.1499C>T
MANE Select
|
NP_001323.1:p.Ala500Val
|
|
NM_001288717.2:c.200C>T
|
NP_001275646.1:p.Ala67Val
|
|
NR_109988.2:n.1354C>T
|
|
|
NM_001364128.2:c.488C>T
|
NP_001351057.1:p.Ala163Val
|
|