ENST00000281928.9:c.5589-5G>T
MANE Select
|
ENSP00000281928.3:n.5589-5G>T
|
|
ENST00000548694.2:n.574G>T
|
|
|
ENST00000648379.1:n.3957-5G>T
|
|
|
ENST00000648737.1:n.5353-5G>T
|
|
|
ENST00000648825.1:n.3774-5G>T
|
|
|
ENST00000648916.1:n.3600-5G>T
|
|
|
ENST00000649607.1:c.3773-5G>T
|
|
|
ENST00000649775.1:c.2078-5G>T
|
|
|
ENST00000650226.1:c.5620G>T
|
ENSP00000496981.1:p.Val1874Phe
|
|
ENST00000281928.7:c.5589-5G>T
|
ENSP00000281928.3:n.5589-5G>T
|
|
ENST00000548694.1:n.574G>T
|
|
|
ENST00000552447.1:c.197G>T
|
|
|
NM_015335.4:c.5589-5G>T
|
NP_056150.1:n.5589-5G>T
|
|
XM_011538080.1:c.5620G>T
|
XP_011536382.1:p.Val1874Phe
|
|
XM_011538081.1:c.5617G>T
|
XP_011536383.1:p.Val1873Phe
|
|
XM_011538082.1:c.5590G>T
|
XP_011536384.1:p.Val1864Phe
|
|
XM_011538080.2:c.5620G>T
|
XP_011536382.1:p.Val1874Phe
|
|
XM_011538081.2:c.5617G>T
|
XP_011536383.1:p.Val1873Phe
|
|
XM_011538082.2:c.5590G>T
|
XP_011536384.1:p.Val1864Phe
|
|
XM_017019090.1:c.5586-5G>T
|
XP_016874579.1:n.5586-5G>T
|
|
NM_015335.5:c.5589-5G>T
MANE Select
|
NP_056150.1:n.5589-5G>T
|
|