ENST00000281928.9:c.5613A>T
MANE Select
|
ENSP00000281928.3:p.Ala1871=
|
|
ENST00000548694.2:n.603A>T
|
|
|
ENST00000648379.1:n.3981A>T
|
|
|
ENST00000648737.1:n.5377A>T
|
|
|
ENST00000648825.1:n.3798A>T
|
|
|
ENST00000648916.1:n.3624A>T
|
|
|
ENST00000649607.1:c.3797A>T
|
|
|
ENST00000649775.1:c.2102A>T
|
|
|
ENST00000650226.1:c.5649A>T
|
ENSP00000496981.1:p.Ala1883=
|
|
ENST00000281928.7:c.5613A>T
|
ENSP00000281928.3:p.Ala1871=
|
|
ENST00000548694.1:n.603A>T
|
|
|
ENST00000552447.1:c.226A>T
|
|
|
NM_015335.4:c.5613A>T
|
NP_056150.1:p.Ala1871=
|
|
XM_011538080.1:c.5649A>T
|
XP_011536382.1:p.Ala1883=
|
|
XM_011538081.1:c.5646A>T
|
XP_011536383.1:p.Ala1882=
|
|
XM_011538082.1:c.5619A>T
|
XP_011536384.1:p.Ala1873=
|
|
XM_011538080.2:c.5649A>T
|
XP_011536382.1:p.Ala1883=
|
|
XM_011538081.2:c.5646A>T
|
XP_011536383.1:p.Ala1882=
|
|
XM_011538082.2:c.5619A>T
|
XP_011536384.1:p.Ala1873=
|
|
XM_017019090.1:c.5610A>T
|
XP_016874579.1:p.Ala1870=
|
|
NM_015335.5:c.5613A>T
MANE Select
|
NP_056150.1:p.Ala1871=
|
|