ENST00000356839.10:c.420G=
MANE Select
|
ENSP00000349297.5:p.Gly140=
|
|
ENST00000322910.9:c.*375G=
|
ENSP00000325395.5:n.*375G=
|
|
ENST00000350303.9:c.354G=
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ENSP00000344152.5:p.Gly118=
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|
ENST00000356839.9:c.420G=
|
ENSP00000349297.5:p.Gly140=
|
|
ENST00000543245.6:c.489G=
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ENSP00000438689.2:p.Gly163=
|
|
ENST00000577191.5:n.497G=
|
|
|
ENST00000577433.5:n.628G=
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|
|
ENST00000577857.5:n.293+171G=
|
|
|
ENST00000579286.5:n.601G=
|
|
|
ENST00000579886.2:c.258G=
|
ENSP00000463246.1:p.Gly86=
|
|
ENST00000580365.1:n.151G=
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|
|
ENST00000581378.5:c.119G=
|
|
|
ENST00000581562.5:n.467G=
|
|
|
ENST00000582056.5:n.603G=
|
|
|
ENST00000582166.1:n.401G=
|
|
|
ENST00000583312.5:c.420G=
|
ENSP00000467920.1:p.Gly140=
|
|
ENST00000584103.5:c.453G=
|
ENSP00000465353.1:p.Gly151=
|
|
NM_000018.3:c.420G=
|
NP_000009.1:p.Gly140=
|
|
NM_001033859.2:c.354G=
|
NP_001029031.1:p.Gly118=
|
|
NM_001270447.1:c.489G=
|
NP_001257376.1:p.Gly163=
|
|
NM_001270448.1:c.192G=
|
NP_001257377.1:p.Gly64=
|
|
XM_006721516.2:c.420G=
|
XP_006721579.2:p.Gly140=
|
|
XM_011523829.1:c.420G=
|
XP_011522131.1:p.Gly140=
|
|
XM_011523830.1:c.420G=
|
XP_011522132.1:p.Gly140=
|
|
XR_934021.1:n.527G=
|
|
|
XR_934022.1:n.527G=
|
|
|
XR_934023.1:n.527G=
|
|
|
XM_006721516.3:c.420G=
|
XP_006721579.2:p.Gly140=
|
|
XM_011523829.2:c.420G=
|
XP_011522131.1:p.Gly140=
|
|
XM_011523830.2:c.420G=
|
XP_011522132.1:p.Gly140=
|
|
XM_024450741.1:c.420G=
|
XP_024306509.1:p.Gly140=
|
|
XR_934021.2:n.479G=
|
|
|
XR_934022.2:n.479G=
|
|
|
XR_934023.2:n.479G=
|
|
|
NM_000018.4:c.420G=
MANE Select
|
NP_000009.1:p.Gly140=
|
|
NM_001033859.3:c.354G=
|
NP_001029031.1:p.Gly118=
|
|
NM_001270447.2:c.489G=
|
NP_001257376.1:p.Gly163=
|
|
NM_001270448.2:c.192G=
|
NP_001257377.1:p.Gly64=
|
|