ENST00000281928.9:c.6051G>C
MANE Select
|
ENSP00000281928.3:p.Gly2017=
|
|
ENST00000548784.2:n.2265G>C
|
|
|
ENST00000648379.1:n.4419G>C
|
|
|
ENST00000648737.1:n.5815G>C
|
|
|
ENST00000648825.1:n.4236G>C
|
|
|
ENST00000648916.1:n.4062G>C
|
|
|
ENST00000649607.1:c.4235G>C
|
|
|
ENST00000649775.1:c.2540G>C
|
|
|
ENST00000650226.1:c.6087G>C
|
ENSP00000496981.1:p.Gly2029=
|
|
ENST00000281928.7:c.6051G>C
|
ENSP00000281928.3:p.Gly2017=
|
|
NM_015335.4:c.6051G>C
|
NP_056150.1:p.Gly2017=
|
|
XM_011538080.1:c.6087G>C
|
XP_011536382.1:p.Gly2029=
|
|
XM_011538081.1:c.6084G>C
|
XP_011536383.1:p.Gly2028=
|
|
XM_011538082.1:c.6057G>C
|
XP_011536384.1:p.Gly2019=
|
|
XM_011538080.2:c.6087G>C
|
XP_011536382.1:p.Gly2029=
|
|
XM_011538081.2:c.6084G>C
|
XP_011536383.1:p.Gly2028=
|
|
XM_011538082.2:c.6057G>C
|
XP_011536384.1:p.Gly2019=
|
|
XM_017019090.1:c.6048G>C
|
XP_016874579.1:p.Gly2016=
|
|
NM_015335.5:c.6051G>C
MANE Select
|
NP_056150.1:p.Gly2017=
|
|