ENST00000480188.2:n.1367G>T
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|
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ENST00000696279.1:c.4653G>T
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|
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ENST00000696280.1:n.4422G>T
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|
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ENST00000696281.1:c.4351G>T
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ENSP00000512521.1:p.Gly1451Trp
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ENST00000697921.1:n.3211G>T
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|
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ENST00000697922.1:c.*4323G>T
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ENSP00000513478.1:n.*4323G>T
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ENST00000697923.1:n.4778G>T
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|
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ENST00000223642.3:c.4333G>T
MANE Select
|
ENSP00000223642.1:p.Gly1445Trp
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ENST00000223642.2:c.4333G>T
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ENSP00000223642.1:p.Gly1445Trp
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NM_001735.2:c.4333G>T , LRG_28t1:c.4333G>T
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NP_001726.2:p.Gly1445Trp
|
|
XM_011518980.1:c.4348G>T
|
XP_011517282.1:p.Gly1450Trp
|
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NM_001317163.1:c.4351G>T
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NP_001304092.1:p.Gly1451Trp
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|
NM_001317163.2:c.4351G>T
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NP_001304092.1:p.Gly1451Trp
|
|
NM_001735.3:c.4333G>T
MANE Select
|
NP_001726.2:p.Gly1445Trp
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