ENST00000355265.7:c.536G>A
MANE Select
|
ENSP00000347409.2:p.Trp179Ter
|
|
ENST00000467543.6:c.*388G>A
|
ENSP00000420011.2:n.*388G>A
|
|
ENST00000355265.6:c.536G>A
|
ENSP00000347409.2:p.Trp179Ter
|
|
ENST00000467543.5:c.479G>A
|
ENSP00000420011.1:p.Trp160Ter
|
|
ENST00000476829.5:c.525+341G>A
|
ENSP00000419889.1:n.525+341G>A
|
|
ENST00000479768.6:n.654G>A
|
|
|
ENST00000494148.1:n.135G>A
|
|
|
NM_000420.2:c.536G>A
|
NP_000411.1:p.Trp179Ter
|
|
XM_005249993.2:c.572G>A
|
XP_005250050.1:p.Trp191Ter
|
|
NM_000420.3:c.536G>A
MANE Select
|
NP_000411.1:p.Trp179Ter
|
|