ENST00000454220.7:c.690G=
|
ENSP00000391905.3:p.Gly230=
|
|
ENST00000703395.1:c.33G=
|
ENSP00000515286.1:p.Gly11=
|
|
ENST00000703396.1:n.514G=
|
|
|
ENST00000703397.1:c.33G=
|
ENSP00000515287.1:p.Gly11=
|
|
ENST00000703398.1:c.612G=
|
ENSP00000515288.1:p.Gly204=
|
|
ENST00000703421.1:n.723G=
|
|
|
ENST00000703422.1:c.546G=
|
ENSP00000515292.1:p.Gly182=
|
|
ENST00000703423.1:c.33G=
|
ENSP00000515293.1:p.Gly11=
|
|
ENST00000322088.11:c.570G=
MANE Select
|
ENSP00000324804.6:p.Gly190=
|
|
ENST00000322088.10:c.570G=
|
ENSP00000324804.6:p.Gly190=
|
|
ENST00000454220.6:c.690G=
|
ENSP00000391905.2:p.Gly230=
|
|
ENST00000462047.1:n.261G=
|
|
|
ENST00000462990.5:c.33G=
|
ENSP00000470504.1:p.Gly11=
|
|
NM_014225.5:c.570G=
|
NP_055040.2:p.Gly190=
|
|
NR_033500.1:n.764G=
|
|
|
NM_001363656.1:c.33G=
|
NP_001350585.1:p.Gly11=
|
|
NM_014225.6:c.570G=
MANE Select
|
NP_055040.2:p.Gly190=
|
|
NM_001363656.2:c.33G=
|
NP_001350585.1:p.Gly11=
|
|
NR_033500.2:n.514G=
|
|
|