ENST00000342245.9:c.957T>G
MANE Select
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ENSP00000340409.4:p.Gly319=
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ENST00000342245.8:c.957T>G
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ENSP00000340409.4:p.Gly319=
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ENST00000526280.1:c.146T>G
|
|
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ENST00000527275.5:c.954T>G
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ENSP00000435350.1:p.Gly318=
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ENST00000530395.1:c.138T>G
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ENSP00000431479.1:p.Gly46=
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ENST00000531303.5:c.438+519T>G
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ENSP00000432625.1:n.438+519T>G
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ENST00000533123.5:c.957T>G
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ENSP00000435950.1:p.Gly319=
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|
ENST00000533196.1:n.391T>G
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|
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ENST00000534405.5:c.957T>G
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ENSP00000434353.1:p.Gly319=
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NM_000543.4:c.957T>G
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NP_000534.3:p.Gly319=
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NM_001007593.2:c.954T>G
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NP_001007594.2:p.Gly318=
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XM_005253075.3:c.957T>G
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XP_005253132.1:p.Gly319=
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XM_011520303.1:c.957T>G
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XP_011518605.1:p.Gly319=
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|
XM_011520304.1:c.957T>G
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XP_011518606.1:p.Gly319=
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XR_930886.1:n.1255T>G
|
|
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NM_001318087.1:c.957T>G
|
NP_001305016.1:p.Gly319=
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|
NM_001318088.1:c.-5T>G
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NP_001305017.1:n.-5T>G
|
|
NM_001365135.1:c.957T>G
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NP_001352064.1:p.Gly319=
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NR_027400.2:n.1142T>G
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NR_134502.1:n.623+519T>G
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|
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XM_011520304.2:c.957T>G
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XP_011518606.1:p.Gly319=
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|
XR_001747940.2:n.1082T>G
|
|
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XR_002957158.1:n.1082T>G
|
|
|
NM_000543.5:c.957T>G
MANE Select
|
NP_000534.3:p.Gly319=
|
|
NM_001007593.3:c.954T>G
|
NP_001007594.2:p.Gly318=
|
|
NM_001318087.2:c.957T>G
|
NP_001305016.1:p.Gly319=
|
|
NM_001318088.2:c.-5T>G
|
NP_001305017.1:n.-5T>G
|
|
NM_001365135.2:c.957T>G
|
NP_001352064.1:p.Gly319=
|
|
NR_027400.3:n.1082T>G
|
|
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NR_134502.2:n.563+519T>G
|
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