ENST00000346342.8:c.1306G>T
MANE Select
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ENSP00000329546.4:p.Gly436Ter
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ENST00000346342.7:c.1306G>T
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ENSP00000329546.3:p.Gly436Ter
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ENST00000375581.3:c.1372G>T
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ENSP00000364731.3:p.Gly458Ter
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ENST00000541084.5:c.1120G>T
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ENSP00000442051.2:p.Gly374Ter
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NM_000131.4:c.1372G>T , LRG_554t1:c.1372G>T
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NP_000122.1:p.Gly458Ter
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NM_001267554.1:c.1120G>T
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NP_001254483.1:p.Gly374Ter
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NM_019616.3:c.1306G>T , LRG_554t2:c.1306G>T
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NP_062562.1:p.Gly436Ter
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NR_051961.1:n.1393G>T
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XM_006719963.2:c.1165G>T
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XP_006720026.1:p.Gly389Ter
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XM_011537474.1:c.1414G>T
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XP_011535776.1:p.Gly472Ter
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XM_011537475.1:c.1228G>T
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XP_011535777.1:p.Gly410Ter
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XM_011537476.1:c.1066G>T
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XP_011535778.1:p.Gly356Ter
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XM_011537477.1:c.1375G>T
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XP_011535779.1:p.Gly459Ter
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XM_006719963.3:c.1210G>T
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XP_006720026.2:p.Gly404Ter
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XM_011537474.2:c.1459G>T
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XP_011535776.2:p.Gly487Ter
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XM_011537475.2:c.1273G>T
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XP_011535777.2:p.Gly425Ter
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XM_011537476.2:c.1066G>T
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XP_011535778.1:p.Gly356Ter
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NM_019616.4:c.1306G>T
MANE Select
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NP_062562.1:p.Gly436Ter
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NR_051961.2:n.1390G>T
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NM_001267554.2:c.1120G>T
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NP_001254483.1:p.Gly374Ter
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