ENST00000366667.6:c.1239G>T
MANE Select
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ENSP00000355627.5:p.Gly413=
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ENST00000679684.1:c.1239G>T
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ENSP00000505981.1:p.Gly413=
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ENST00000679738.1:c.1239G>T
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ENSP00000505063.1:p.Gly413=
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ENST00000679802.1:c.*698G>T
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ENSP00000505184.1:n.*698G>T
|
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ENST00000679854.1:n.5544G>T
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ENST00000679957.1:c.1233+6G>T
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ENSP00000506646.1:n.1233+6G>T
|
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ENST00000680041.1:c.1239G>T
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ENSP00000504866.1:p.Gly413=
|
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ENST00000680783.1:c.829+5799G>T
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ENSP00000506329.1:n.829+5799G>T
|
|
ENST00000681269.1:c.1239G>T
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ENSP00000505985.1:p.Gly413=
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ENST00000681347.1:n.3345G>T
|
|
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ENST00000681514.1:c.1239G>T
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ENSP00000505963.1:p.Gly413=
|
|
ENST00000681772.1:c.*733G>T
|
ENSP00000505829.1:n.*733G>T
|
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ENST00000366667.4:c.1266G>T
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ENSP00000355627.4:p.Gly422=
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NM_000029.3:c.1266G>T
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NP_000020.1:p.Gly422=
|
|
NM_000029.4:c.1266G>T
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NP_000020.1:p.Gly422=
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NM_001382817.3:c.1239G>T
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NP_001369746.2:p.Gly413=
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|
NM_001384479.1:c.1239G>T
MANE Select
|
NP_001371408.1:p.Gly413=
|
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