ENST00000520439.3:c.636T>C
MANE Select
|
ENSP00000430676.1:p.Gly212=
|
|
ENST00000523477.2:n.460T>C
|
|
|
ENST00000647605.1:c.384T>C
|
ENSP00000497893.1:p.Gly128=
|
|
ENST00000648164.1:c.636T>C
|
ENSP00000498198.1:p.Gly212=
|
|
ENST00000648481.1:n.497T>C
|
|
|
ENST00000649473.1:c.600T>C
|
ENSP00000498160.1:p.Gly200=
|
|
ENST00000649696.1:c.384T>C
|
ENSP00000497127.1:p.Gly128=
|
|
ENST00000650269.1:c.636T>C
|
ENSP00000496915.1:p.Gly212=
|
|
ENST00000303015.2:c.636T>C
|
ENSP00000302166.1:p.Gly212=
|
|
ENST00000520439.1:c.636T>C
|
ENSP00000430676.1:p.Gly212=
|
|
ENST00000522317.5:c.636T>C
|
ENSP00000429847.1:p.Gly212=
|
|
NM_001282534.1:c.636T>C
|
NP_001269463.1:p.Gly212=
|
|
NR_104210.1:n.700T>C
|
|
|
XM_011517101.1:c.636T>C
|
XP_011515403.1:p.Gly212=
|
|
XM_011517102.1:c.636T>C
|
XP_011515404.1:p.Gly212=
|
|
XM_011517103.1:c.306T>C
|
XP_011515405.1:p.Gly102=
|
|
XM_011517101.2:c.636T>C
|
XP_011515403.1:p.Gly212=
|
|
XM_011517102.2:c.636T>C
|
XP_011515404.1:p.Gly212=
|
|
XM_011517103.2:c.306T>C
|
XP_011515405.1:p.Gly102=
|
|
XM_017013530.1:c.306T>C
|
XP_016869019.1:p.Gly102=
|
|
XM_017013531.1:c.306T>C
|
XP_016869020.1:p.Gly102=
|
|
NM_001282534.2:c.636T>C
MANE Select
|
NP_001269463.1:p.Gly212=
|
|
NR_104210.2:n.767T>C
|
|
|