ENST00000703783.1:n.574T>C
|
|
|
ENST00000703785.1:n.655T>C
|
|
|
ENST00000262464.9:c.3790T>C
MANE Select
|
ENSP00000262464.4:p.Tyr1264His
|
|
ENST00000262464.8:c.3790T>C
|
ENSP00000262464.4:p.Tyr1264His
|
|
ENST00000507835.5:c.340T>C
|
ENSP00000426839.1:p.Tyr114His
|
|
ENST00000508053.5:c.3790T>C
|
ENSP00000424571.1:p.Tyr1264His
|
|
ENST00000508989.5:c.3691T>C
|
ENSP00000425596.1:p.Tyr1231His
|
|
ENST00000619499.4:c.3787T>C
|
ENSP00000482132.1:p.Tyr1263His
|
|
NM_001999.3:c.3790T>C
|
NP_001990.2:p.Tyr1264His
|
|
XM_017009228.2:c.3637T>C
|
XP_016864717.1:p.Tyr1213His
|
|
NM_001999.4:c.3790T>C
MANE Select
|
NP_001990.2:p.Tyr1264His
|
|