ENST00000703783.1:n.377G>T
|
|
|
ENST00000703785.1:n.458G>T
|
|
|
ENST00000262464.9:c.3593G>T
MANE Select
|
ENSP00000262464.4:p.Cys1198Phe
|
|
ENST00000262464.8:c.3593G>T
|
ENSP00000262464.4:p.Cys1198Phe
|
|
ENST00000507835.5:c.143G>T
|
ENSP00000426839.1:p.Cys48Phe
|
|
ENST00000508053.5:c.3593G>T
|
ENSP00000424571.1:p.Cys1198Phe
|
|
ENST00000508989.5:c.3494G>T
|
ENSP00000425596.1:p.Cys1165Phe
|
|
ENST00000619499.4:c.3590G>T
|
ENSP00000482132.1:p.Cys1197Phe
|
|
NM_001999.3:c.3593G>T
|
NP_001990.2:p.Cys1198Phe
|
|
XM_017009228.2:c.3440G>T
|
XP_016864717.1:p.Cys1147Phe
|
|
NM_001999.4:c.3593G>T
MANE Select
|
NP_001990.2:p.Cys1198Phe
|
|