ENST00000379644.9:c.1384T>C
MANE Select
|
ENSP00000368965.4:p.Tyr462His
|
|
ENST00000379644.8:c.1384T>C
|
ENSP00000368965.4:p.Tyr462His
|
|
ENST00000520678.1:n.317T>C
|
|
|
ENST00000521576.1:c.535T>C
|
ENSP00000429029.1:p.Tyr179His
|
|
ENST00000524016.5:c.488T>C
|
|
|
NM_152419.2:c.1384T>C
|
NP_689632.2:p.Tyr462His
|
|
XM_005273409.1:c.1384T>C
|
XP_005273466.1:p.Tyr462His
|
|
XM_005273410.1:c.1384T>C
|
XP_005273467.1:p.Tyr462His
|
|
XM_005273411.1:c.1192T>C
|
XP_005273468.1:p.Tyr398His
|
|
XM_005273412.2:c.1384T>C
|
XP_005273469.1:p.Tyr462His
|
|
NM_001363227.1:c.1384T>C
|
NP_001350156.1:p.Tyr462His
|
|
NM_001363228.1:c.1192T>C
|
NP_001350157.1:p.Tyr398His
|
|
NM_001363229.1:c.520T>C
|
NP_001350158.1:p.Tyr174His
|
|
XM_005273412.4:c.1384T>C
|
XP_005273469.1:p.Tyr462His
|
|
NM_152419.3:c.1384T>C
MANE Select
|
NP_689632.2:p.Tyr462His
|
|
NM_001363227.2:c.1384T>C
|
NP_001350156.1:p.Tyr462His
|
|
NM_001363228.2:c.1192T>C
|
NP_001350157.1:p.Tyr398His
|
|
NM_001363229.2:c.520T>C
|
NP_001350158.1:p.Tyr174His
|
|