ENST00000703783.1:n.376T>G
|
|
|
ENST00000703785.1:n.457T>G
|
|
|
ENST00000262464.9:c.3592T>G
MANE Select
|
ENSP00000262464.4:p.Cys1198Gly
|
|
ENST00000262464.8:c.3592T>G
|
ENSP00000262464.4:p.Cys1198Gly
|
|
ENST00000507835.5:c.142T>G
|
ENSP00000426839.1:p.Cys48Gly
|
|
ENST00000508053.5:c.3592T>G
|
ENSP00000424571.1:p.Cys1198Gly
|
|
ENST00000508989.5:c.3493T>G
|
ENSP00000425596.1:p.Cys1165Gly
|
|
ENST00000619499.4:c.3589T>G
|
ENSP00000482132.1:p.Cys1197Gly
|
|
NM_001999.3:c.3592T>G
|
NP_001990.2:p.Cys1198Gly
|
|
XM_017009228.2:c.3439T>G
|
XP_016864717.1:p.Cys1147Gly
|
|
NM_001999.4:c.3592T>G
MANE Select
|
NP_001990.2:p.Cys1198Gly
|
|