ENST00000372391.7:c.3528C>T
MANE Select
|
ENSP00000361467.2:p.Gly1176=
|
|
ENST00000372391.6:c.3528C>T
|
ENSP00000361467.2:p.Gly1176=
|
|
ENST00000424842.5:c.411C>T
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ENSP00000394797.1:p.Gly137=
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ENST00000459739.5:n.583C>T
|
|
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ENST00000463362.5:n.156C>T
|
|
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ENST00000468332.6:c.3530C>T
|
ENSP00000473298.1:n.3530C>T
|
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ENST00000475613.6:n.3365C>T
|
|
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ENST00000476354.2:n.558C>T
|
|
|
NM_004747.3:c.3528C>T
|
NP_004738.3:p.Gly1176=
|
|
XM_005270276.3:c.3516C>T
|
XP_005270333.1:p.Gly1172=
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XM_006718056.2:c.2508C>T
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XP_006718119.1:p.Gly836=
|
|
XM_006718057.2:c.3528C>T
|
XP_006718120.1:p.Gly1176=
|
|
XM_011540341.1:c.3351C>T
|
XP_011538643.1:p.Gly1117=
|
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XM_011540342.1:c.3258C>T
|
XP_011538644.1:p.Gly1086=
|
|
XM_011540343.1:c.3198C>T
|
XP_011538645.1:p.Gly1066=
|
|
XM_011540344.1:c.3192C>T
|
XP_011538646.1:p.Gly1064=
|
|
XM_011540345.1:c.3063C>T
|
XP_011538647.1:p.Gly1021=
|
|
XM_011540346.1:c.3528C>T
|
XP_011538648.1:p.Gly1176=
|
|
XM_011540347.1:c.2610C>T
|
XP_011538649.1:p.Gly870=
|
|
XR_945874.1:n.3781C>T
|
|
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XM_005270276.4:c.3516C>T
|
XP_005270333.1:p.Gly1172=
|
|
XM_006718056.3:c.2508C>T
|
XP_006718119.1:p.Gly836=
|
|
XM_006718057.3:c.3528C>T
|
XP_006718120.1:p.Gly1176=
|
|
XM_011540341.3:c.3351C>T
|
XP_011538643.1:p.Gly1117=
|
|
XM_011540344.2:c.3192C>T
|
XP_011538646.1:p.Gly1064=
|
|
XM_011540346.2:c.3528C>T
|
XP_011538648.1:p.Gly1176=
|
|
XM_011540347.2:c.2610C>T
|
XP_011538649.1:p.Gly870=
|
|
XM_017016913.1:c.3246C>T
|
XP_016872402.1:p.Gly1082=
|
|
XM_017016914.1:c.3198C>T
|
XP_016872403.1:p.Gly1066=
|
|
XM_017016915.1:c.2610C>T
|
XP_016872404.1:p.Gly870=
|
|
XM_024448250.1:c.2073C>T
|
XP_024304018.1:p.Gly691=
|
|
XR_945874.2:n.3792C>T
|
|
|
NM_004747.4:c.3528C>T
MANE Select
|
NP_004738.3:p.Gly1176=
|
|