ENST00000324071.10:c.1253G=
MANE Select
|
ENSP00000324648.2:p.Gly418=
|
|
ENST00000598834.2:c.1177-199G=
|
|
|
ENST00000324071.8:c.1253G=
|
ENSP00000324648.2:p.Gly418=
|
|
ENST00000593831.1:c.545G=
|
ENSP00000470582.1:p.Gly182=
|
|
ENST00000597612.1:n.647+289G=
|
|
|
NM_000767.4:c.1253G=
|
NP_000758.1:p.Gly418=
|
|
XM_005258569.3:c.1152+289G=
|
XP_005258626.1:n.1152+289G=
|
|
XM_006723050.2:c.1253G=
|
XP_006723113.1:p.Gly418=
|
|
XM_011526546.1:c.1153-42G=
|
XP_011524848.1:n.1153-42G=
|
|
XM_011526547.1:c.1153-199G=
|
XP_011524849.1:n.1153-199G=
|
|
XM_011526548.1:c.773G=
|
XP_011524850.1:p.Gly258=
|
|
XM_011526549.1:c.662G=
|
XP_011524851.1:p.Gly221=
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|
XM_011526550.1:c.653G=
|
XP_011524852.1:p.Gly218=
|
|
NM_000767.5:c.1253G=
MANE Select
|
NP_000758.1:p.Gly418=
|
|