ENST00000703783.1:n.509A>G
|
|
|
ENST00000703785.1:n.590A>G
|
|
|
ENST00000262464.9:c.3725A>G
MANE Select
|
ENSP00000262464.4:p.Asp1242Gly
|
|
ENST00000262464.8:c.3725A>G
|
ENSP00000262464.4:p.Asp1242Gly
|
|
ENST00000507835.5:c.275A>G
|
ENSP00000426839.1:p.Asp92Gly
|
|
ENST00000508053.5:c.3725A>G
|
ENSP00000424571.1:p.Asp1242Gly
|
|
ENST00000508989.5:c.3626A>G
|
ENSP00000425596.1:p.Asp1209Gly
|
|
ENST00000619499.4:c.3722A>G
|
ENSP00000482132.1:p.Asp1241Gly
|
|
NM_001999.3:c.3725A>G
|
NP_001990.2:p.Asp1242Gly
|
|
XM_017009228.2:c.3572A>G
|
XP_016864717.1:p.Asp1191Gly
|
|
NM_001999.4:c.3725A>G
MANE Select
|
NP_001990.2:p.Asp1242Gly
|
|