ENST00000220420.10:c.780C>T
MANE Select
|
ENSP00000220420.5:p.Ala260=
|
|
ENST00000635871.1:n.249C>T
|
|
|
ENST00000220420.9:c.780C>T
|
ENSP00000220420.5:p.Ala260=
|
|
ENST00000349114.8:c.534C>T
|
ENSP00000220419.8:p.Ala178=
|
|
ENST00000610827.4:c.777C>T
|
ENSP00000479732.1:p.Ala259=
|
|
ENST00000611276.4:c.531C>T
|
ENSP00000482542.1:p.Ala177=
|
|
ENST00000622115.1:c.783C>T
|
ENSP00000479638.1:p.Ala261=
|
|
NM_004245.3:c.534C>T
|
NP_004236.1:p.Ala178=
|
|
NM_201631.3:c.780C>T
|
NP_963925.2:p.Ala260=
|
|
XM_011522229.1:c.780C>T
|
XP_011520531.1:p.Ala260=
|
|
XR_931948.1:n.954C>T
|
|
|
NM_004245.4:c.534C>T
|
NP_004236.1:p.Ala178=
|
|
NM_201631.4:c.780C>T
MANE Select
|
NP_963925.2:p.Ala260=
|
|