ENST00000298139.7:c.4284A>C
MANE Select
|
ENSP00000298139.5:p.Gly1428=
|
|
ENST00000650667.1:c.*3898A>C
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ENSP00000498593.1:n.*3898A>C
|
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ENST00000651946.1:n.508A>C
|
|
|
ENST00000298139.5:c.4284A>C
|
ENSP00000298139.5:p.Gly1428=
|
|
ENST00000521620.5:n.2917A>C
|
|
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NM_000553.4:c.4284A>C , LRG_524t1:c.4284A>C
|
NP_000544.2:p.Gly1428=
|
|
XM_011544639.1:c.4203A>C
|
XP_011542941.1:p.Gly1401=
|
|
XM_011544640.1:c.2685A>C
|
XP_011542942.1:p.Gly895=
|
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XR_949643.1:n.88-1769T>G
|
|
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XR_949644.1:n.88-1769T>G
|
|
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XR_949645.1:n.88-1769T>G
|
|
|
XR_949646.1:n.88-1769T>G
|
|
|
XR_949647.1:n.701-1769T>G
|
|
|
XR_949648.1:n.603-1769T>G
|
|
|
NM_000553.5:c.4284A>C
|
NP_000544.2:p.Gly1428=
|
|
XM_011544639.3:c.4203A>C
|
XP_011542941.1:p.Gly1401=
|
|
XM_024447265.1:c.4074A>C
|
XP_024303033.1:p.Gly1358=
|
|
NM_000553.6:c.4284A>C
MANE Select
|
NP_000544.2:p.Gly1428=
|
|