ENST00000281928.9:c.5691A>C
MANE Select
|
ENSP00000281928.3:p.Val1897=
|
|
ENST00000548694.2:n.681A>C
|
|
|
ENST00000648379.1:n.4059A>C
|
|
|
ENST00000648737.1:n.5455A>C
|
|
|
ENST00000648825.1:n.3876A>C
|
|
|
ENST00000648916.1:n.3702A>C
|
|
|
ENST00000649607.1:c.3875A>C
|
|
|
ENST00000649775.1:c.2180A>C
|
|
|
ENST00000650226.1:c.5727A>C
|
ENSP00000496981.1:p.Val1909=
|
|
ENST00000281928.7:c.5691A>C
|
ENSP00000281928.3:p.Val1897=
|
|
ENST00000548694.1:n.681A>C
|
|
|
ENST00000552447.1:c.304A>C
|
|
|
NM_015335.4:c.5691A>C
|
NP_056150.1:p.Val1897=
|
|
XM_011538080.1:c.5727A>C
|
XP_011536382.1:p.Val1909=
|
|
XM_011538081.1:c.5724A>C
|
XP_011536383.1:p.Val1908=
|
|
XM_011538082.1:c.5697A>C
|
XP_011536384.1:p.Val1899=
|
|
XM_011538080.2:c.5727A>C
|
XP_011536382.1:p.Val1909=
|
|
XM_011538081.2:c.5724A>C
|
XP_011536383.1:p.Val1908=
|
|
XM_011538082.2:c.5697A>C
|
XP_011536384.1:p.Val1899=
|
|
XM_017019090.1:c.5688A>C
|
XP_016874579.1:p.Val1896=
|
|
NM_015335.5:c.5691A>C
MANE Select
|
NP_056150.1:p.Val1897=
|
|