ENST00000281928.9:c.5646G>A
MANE Select
|
ENSP00000281928.3:p.Trp1882Ter
|
|
ENST00000548694.2:n.636G>A
|
|
|
ENST00000648379.1:n.4014G>A
|
|
|
ENST00000648737.1:n.5410G>A
|
|
|
ENST00000648825.1:n.3831G>A
|
|
|
ENST00000648916.1:n.3657G>A
|
|
|
ENST00000649607.1:c.3830G>A
|
|
|
ENST00000649775.1:c.2135G>A
|
|
|
ENST00000650226.1:c.5682G>A
|
ENSP00000496981.1:p.Trp1894Ter
|
|
ENST00000281928.7:c.5646G>A
|
ENSP00000281928.3:p.Trp1882Ter
|
|
ENST00000548694.1:n.636G>A
|
|
|
ENST00000552447.1:c.259G>A
|
|
|
NM_015335.4:c.5646G>A
|
NP_056150.1:p.Trp1882Ter
|
|
XM_011538080.1:c.5682G>A
|
XP_011536382.1:p.Trp1894Ter
|
|
XM_011538081.1:c.5679G>A
|
XP_011536383.1:p.Trp1893Ter
|
|
XM_011538082.1:c.5652G>A
|
XP_011536384.1:p.Trp1884Ter
|
|
XM_011538080.2:c.5682G>A
|
XP_011536382.1:p.Trp1894Ter
|
|
XM_011538081.2:c.5679G>A
|
XP_011536383.1:p.Trp1893Ter
|
|
XM_011538082.2:c.5652G>A
|
XP_011536384.1:p.Trp1884Ter
|
|
XM_017019090.1:c.5643G>A
|
XP_016874579.1:p.Trp1881Ter
|
|
NM_015335.5:c.5646G>A
MANE Select
|
NP_056150.1:p.Trp1882Ter
|
|