ENST00000281928.9:c.5637A>T
MANE Select
|
ENSP00000281928.3:p.Leu1879Phe
|
|
ENST00000548694.2:n.627A>T
|
|
|
ENST00000648379.1:n.4005A>T
|
|
|
ENST00000648737.1:n.5401A>T
|
|
|
ENST00000648825.1:n.3822A>T
|
|
|
ENST00000648916.1:n.3648A>T
|
|
|
ENST00000649607.1:c.3821A>T
|
|
|
ENST00000649775.1:c.2126A>T
|
|
|
ENST00000650226.1:c.5673A>T
|
ENSP00000496981.1:p.Leu1891Phe
|
|
ENST00000281928.7:c.5637A>T
|
ENSP00000281928.3:p.Leu1879Phe
|
|
ENST00000548694.1:n.627A>T
|
|
|
ENST00000552447.1:c.250A>T
|
|
|
NM_015335.4:c.5637A>T
|
NP_056150.1:p.Leu1879Phe
|
|
XM_011538080.1:c.5673A>T
|
XP_011536382.1:p.Leu1891Phe
|
|
XM_011538081.1:c.5670A>T
|
XP_011536383.1:p.Leu1890Phe
|
|
XM_011538082.1:c.5643A>T
|
XP_011536384.1:p.Leu1881Phe
|
|
XM_011538080.2:c.5673A>T
|
XP_011536382.1:p.Leu1891Phe
|
|
XM_011538081.2:c.5670A>T
|
XP_011536383.1:p.Leu1890Phe
|
|
XM_011538082.2:c.5643A>T
|
XP_011536384.1:p.Leu1881Phe
|
|
XM_017019090.1:c.5634A>T
|
XP_016874579.1:p.Leu1878Phe
|
|
NM_015335.5:c.5637A>T
MANE Select
|
NP_056150.1:p.Leu1879Phe
|
|