ENST00000344209.10:c.1054C>T
MANE Select
|
ENSP00000345667.5:p.Gln352Ter
|
|
ENST00000460554.2:n.1004C>T
|
|
|
ENST00000642615.1:c.*237C>T
|
ENSP00000495499.1:n.*237C>T
|
|
ENST00000273691.7:c.922C>T
|
ENSP00000273691.3:p.Gln308Ter
|
|
ENST00000344209.9:c.1054C>T
|
ENSP00000345667.5:p.Gln352Ter
|
|
ENST00000393631.5:c.787C>T
|
ENSP00000377251.1:p.Gln263Ter
|
|
ENST00000460554.1:n.1156C>T
|
|
|
ENST00000462014.1:c.958C>T
|
ENSP00000419414.1:p.Gln320Ter
|
|
NM_001199799.1:c.1054C>T
|
NP_001186728.1:p.Gln352Ter
|
|
NM_001199800.1:c.787C>T
|
NP_001186729.1:p.Gln263Ter
|
|
NM_175924.3:c.922C>T
|
NP_787120.1:p.Gln308Ter
|
|
XM_005247389.3:c.958C>T
|
XP_005247446.1:p.Gln320Ter
|
|
XM_011512738.1:c.1054C>T
|
XP_011511040.1:p.Gln352Ter
|
|
XM_011512739.1:c.517C>T
|
XP_011511041.1:p.Gln173Ter
|
|
XM_005247389.4:c.958C>T
|
XP_005247446.1:p.Gln320Ter
|
|
XM_011512738.2:c.1054C>T
|
XP_011511040.1:p.Gln352Ter
|
|
XM_011512739.2:c.517C>T
|
XP_011511041.1:p.Gln173Ter
|
|
NM_001199799.2:c.1054C>T
MANE Select
|
NP_001186728.1:p.Gln352Ter
|
|
NM_001199800.2:c.787C>T
|
NP_001186729.1:p.Gln263Ter
|
|
NM_175924.4:c.922C>T
|
NP_787120.1:p.Gln308Ter
|
|