|
NM_019892.6:c.1795C>T
MANE Select
|
NP_063945.2:p.Arg599Ter
|
|
ENST00000371712.4:c.1795C>T
MANE Select
|
ENSP00000360777.3:p.Arg599Ter
|
|
NM_001318502.1:c.1792C>T
|
NP_001305431.1:p.Arg598Ter
|
|
NM_001318502.2:c.1792C>T
|
NP_001305431.1:p.Arg598Ter
|
|
NM_019892.4:c.1795C>T
|
NP_063945.2:p.Arg599Ter
|
|
NM_019892.5:c.1795C>T
|
NP_063945.2:p.Arg599Ter
|
|
ENST00000371712.3:c.1795C>T
|
ENSP00000360777.3:p.Arg599Ter
|
|
ENST00000676019.1:c.1693C>T
|
ENSP00000501984.1:p.Arg565Ter
|
|
XM_005266094.2:c.1792C>T
|
XP_005266151.1:p.Arg598Ter
|
|
XM_017014926.1:c.1795C>T
|
XP_016870415.1:p.Arg599Ter
|
|
XR_929828.2:n.2400C>T
|
|