ENST00000371270.6:c.410G=
MANE Select
|
ENSP00000360317.3:p.Gly137=
|
|
ENST00000371270.5:c.410G=
|
ENSP00000360317.3:p.Gly137=
|
|
ENST00000479946.2:n.714G=
|
|
|
ENST00000490994.6:c.*196G=
|
ENSP00000433314.1:n.*196G=
|
|
ENST00000525991.5:c.285G=
|
ENSP00000433842.1:p.Gly95=
|
|
ENST00000526814.5:n.665G=
|
|
|
ENST00000527420.5:c.410G=
|
ENSP00000433191.1:p.Gly137=
|
|
ENST00000527953.5:n.665G=
|
|
|
ENST00000533320.5:n.644G=
|
|
|
ENST00000535898.5:c.104G=
|
ENSP00000445062.1:p.Gly35=
|
|
ENST00000539050.5:c.200G=
|
ENSP00000442343.2:p.Gly67=
|
|
ENST00000623108.3:c.200G=
|
ENSP00000485110.1:p.Gly67=
|
|
ENST00000628935.1:c.152G=
|
ENSP00000487145.1:p.Gly51=
|
|
NM_000770.3:c.410G=
MANE Select
|
NP_000761.3:p.Gly137=
|
|
NM_001198853.1:c.200G=
|
NP_001185782.1:p.Gly67=
|
|
NM_001198854.1:c.104G=
|
NP_001185783.1:p.Gly35=
|
|
NM_001198855.1:c.200G=
|
NP_001185784.1:p.Gly67=
|
|
XR_945610.1:n.506G=
|
|
|