ENST00000281928.9:c.2543G>T
MANE Select
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ENSP00000281928.3:p.Gly848Val
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ENST00000548743.2:c.2513G>T
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ENSP00000448553.2:p.Gly838Val
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ENST00000549786.2:c.1971G>T
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ENST00000648173.1:n.1338G>T
|
|
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ENST00000648379.1:n.911G>T
|
|
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ENST00000648737.1:n.2307G>T
|
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ENST00000648916.1:n.554G>T
|
|
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ENST00000649607.1:c.730G>T
|
|
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ENST00000650226.1:c.2543G>T
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ENSP00000496981.1:p.Gly848Val
|
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ENST00000281928.7:c.2543G>T
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ENSP00000281928.3:p.Gly848Val
|
|
NM_015335.4:c.2543G>T
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NP_056150.1:p.Gly848Val
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XM_011538080.1:c.2543G>T
|
XP_011536382.1:p.Gly848Val
|
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XM_011538081.1:c.2543G>T
|
XP_011536383.1:p.Gly848Val
|
|
XM_011538082.1:c.2513G>T
|
XP_011536384.1:p.Gly838Val
|
|
XM_011538080.2:c.2543G>T
|
XP_011536382.1:p.Gly848Val
|
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XM_011538081.2:c.2543G>T
|
XP_011536383.1:p.Gly848Val
|
|
XM_011538082.2:c.2513G>T
|
XP_011536384.1:p.Gly838Val
|
|
XM_017019090.1:c.2543G>T
|
XP_016874579.1:p.Gly848Val
|
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NM_015335.5:c.2543G>T
MANE Select
|
NP_056150.1:p.Gly848Val
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