ENST00000281928.9:c.5639G>C
MANE Select
|
ENSP00000281928.3:p.Trp1880Ser
|
|
ENST00000548694.2:n.629G>C
|
|
|
ENST00000648379.1:n.4007G>C
|
|
|
ENST00000648737.1:n.5403G>C
|
|
|
ENST00000648825.1:n.3824G>C
|
|
|
ENST00000648916.1:n.3650G>C
|
|
|
ENST00000649607.1:c.3823G>C
|
|
|
ENST00000649775.1:c.2128G>C
|
|
|
ENST00000650226.1:c.5675G>C
|
ENSP00000496981.1:p.Trp1892Ser
|
|
ENST00000281928.7:c.5639G>C
|
ENSP00000281928.3:p.Trp1880Ser
|
|
ENST00000548694.1:n.629G>C
|
|
|
ENST00000552447.1:c.252G>C
|
|
|
NM_015335.4:c.5639G>C
|
NP_056150.1:p.Trp1880Ser
|
|
XM_011538080.1:c.5675G>C
|
XP_011536382.1:p.Trp1892Ser
|
|
XM_011538081.1:c.5672G>C
|
XP_011536383.1:p.Trp1891Ser
|
|
XM_011538082.1:c.5645G>C
|
XP_011536384.1:p.Trp1882Ser
|
|
XM_011538080.2:c.5675G>C
|
XP_011536382.1:p.Trp1892Ser
|
|
XM_011538081.2:c.5672G>C
|
XP_011536383.1:p.Trp1891Ser
|
|
XM_011538082.2:c.5645G>C
|
XP_011536384.1:p.Trp1882Ser
|
|
XM_017019090.1:c.5636G>C
|
XP_016874579.1:p.Trp1879Ser
|
|
NM_015335.5:c.5639G>C
MANE Select
|
NP_056150.1:p.Trp1880Ser
|
|