ENST00000350026.11:c.2766C>T
|
ENSP00000055163.8:p.Asn922=
|
|
ENST00000414678.8:c.2676C>T
|
ENSP00000412835.3:p.Asn892=
|
|
ENST00000637015.2:c.2766C>T
|
ENSP00000489729.2:p.Asn922=
|
|
ENST00000319584.11:c.780C>T
|
ENSP00000313006.7:p.Asn260=
|
|
ENST00000346085.10:c.2805C>T
|
ENSP00000344546.5:p.Asn935=
|
|
ENST00000350026.10:c.2517C>T
|
ENSP00000055163.7:p.Asn839=
|
|
ENST00000414678.7:c.924C>T
|
ENSP00000412835.2:p.Asn308=
|
|
ENST00000452544.2:n.667C>T
|
|
|
ENST00000635849.1:c.87C>T
|
ENSP00000490948.1:p.Asn29=
|
|
ENST00000636930.2:c.2766C>T
MANE Select
|
ENSP00000490491.2:p.Asn922=
|
|
ENST00000637015.1:c.5C>T
|
|
|
ENST00000637810.1:c.267C>T
|
ENSP00000489636.1:p.Asn89=
|
|
ENST00000637904.1:c.267C>T
|
ENSP00000490550.1:p.Asn89=
|
|
ENST00000647938.1:c.2556C>T
|
ENSP00000498155.1:p.Asn852=
|
|
ENST00000674190.1:n.1515C>T
|
|
|
ENST00000319584.10:c.783C>T
|
ENSP00000313006.6:p.Asn261=
|
|
ENST00000346085.9:c.2556C>T
|
ENSP00000344546.4:p.Asn852=
|
|
ENST00000350026.9:c.2517C>T
|
ENSP00000055163.7:p.Asn839=
|
|
ENST00000414678.6:c.924C>T
|
ENSP00000412835.2:p.Asn308=
|
|
ENST00000452544.1:n.613C>T
|
|
|
NM_017519.2:c.2517C>T
|
NP_059989.2:p.Asn839=
|
|
NM_020732.3:c.2556C>T
|
NP_065783.3:p.Asn852=
|
|
XM_005267069.3:c.2517C>T
|
XP_005267126.2:p.Asn839=
|
|
XM_011535984.1:c.1467C>T
|
XP_011534286.1:p.Asn489=
|
|
XM_011535985.1:c.1287C>T
|
XP_011534287.1:p.Asn429=
|
|
XM_011535986.1:c.1047C>T
|
XP_011534288.1:p.Asn349=
|
|
XM_011535987.1:c.666C>T
|
XP_011534289.1:p.Asn222=
|
|
XM_011535988.1:c.-20+15421C>T
|
XP_011534290.1:n.-20+15421C>T
|
|
NM_001346813.1:c.2517C>T
|
NP_001333742.1:p.Asn839=
|
|
NM_001363725.1:c.267C>T
|
NP_001350654.1:p.Asn89=
|
|
XM_011535984.2:c.2598C>T
|
XP_011534286.2:p.Asn866=
|
|
XM_011535988.3:c.-20+15421C>T
|
XP_011534290.1:n.-20+15421C>T
|
|
XM_017011103.2:c.2598C>T
|
XP_016866592.1:p.Asn866=
|
|
XM_017011104.1:c.2598C>T
|
XP_016866593.1:p.Asn866=
|
|
XM_017011105.2:c.2598C>T
|
XP_016866594.1:p.Asn866=
|
|
XM_017011106.2:c.2598C>T
|
XP_016866595.1:p.Asn866=
|
|
XM_017011107.2:c.2418C>T
|
XP_016866596.1:p.Asn806=
|
|
XR_002956289.1:n.2681C>T
|
|
|
NM_001363725.2:c.267C>T
|
NP_001350654.1:p.Asn89=
|
|
NM_001371656.1:c.2805C>T
|
NP_001358585.1:p.Asn935=
|
|
NM_001374820.1:c.2805C>T
|
NP_001361749.1:p.Asn935=
|
|
NM_001374828.1:c.2766C>T
MANE Select
|
NP_001361757.1:p.Asn922=
|
|
NM_017519.3:c.2766C>T
|
NP_059989.3:p.Asn922=
|
|