ENST00000703783.1:n.1125C>A
|
|
|
ENST00000703785.1:n.1206C>A
|
|
|
ENST00000262464.9:c.4341C>A
MANE Select
|
ENSP00000262464.4:p.Cys1447Ter
|
|
ENST00000262464.8:c.4341C>A
|
ENSP00000262464.4:p.Cys1447Ter
|
|
ENST00000507835.5:c.891C>A
|
ENSP00000426839.1:p.Cys297Ter
|
|
ENST00000508053.5:c.4341C>A
|
ENSP00000424571.1:p.Cys1447Ter
|
|
ENST00000508989.5:c.4242C>A
|
ENSP00000425596.1:p.Cys1414Ter
|
|
ENST00000619499.4:c.4338C>A
|
ENSP00000482132.1:p.Cys1446Ter
|
|
NM_001999.3:c.4341C>A
|
NP_001990.2:p.Cys1447Ter
|
|
XM_017009228.2:c.4188C>A
|
XP_016864717.1:p.Cys1396Ter
|
|
NM_001999.4:c.4341C>A
MANE Select
|
NP_001990.2:p.Cys1447Ter
|
|