ENST00000346342.8:c.1288C=
MANE Select
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ENSP00000329546.4:p.Arg430=
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|
ENST00000346342.7:c.1288C=
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ENSP00000329546.3:p.Arg430=
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|
ENST00000375581.3:c.1354C=
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ENSP00000364731.3:p.Arg452=
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ENST00000541084.5:c.1102C=
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ENSP00000442051.2:p.Arg368=
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NM_000131.4:c.1354C= , LRG_554t1:c.1354C=
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NP_000122.1:p.Arg452=
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|
NM_001267554.1:c.1102C=
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NP_001254483.1:p.Arg368=
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|
NM_019616.3:c.1288C= , LRG_554t2:c.1288C=
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NP_062562.1:p.Arg430=
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NR_051961.1:n.1375C=
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|
|
XM_006719963.2:c.1147C=
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XP_006720026.1:p.Arg383=
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XM_011537474.1:c.1396C=
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XP_011535776.1:p.Arg466=
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|
XM_011537475.1:c.1210C=
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XP_011535777.1:p.Arg404=
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XM_011537476.1:c.1048C=
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XP_011535778.1:p.Arg350=
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|
XM_011537477.1:c.1357C=
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XP_011535779.1:p.Arg453=
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|
XM_006719963.3:c.1192C=
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XP_006720026.2:p.Arg398=
|
|
XM_011537474.2:c.1441C=
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XP_011535776.2:p.Arg481=
|
|
XM_011537475.2:c.1255C=
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XP_011535777.2:p.Arg419=
|
|
XM_011537476.2:c.1048C=
|
XP_011535778.1:p.Arg350=
|
|
NM_019616.4:c.1288C=
MANE Select
|
NP_062562.1:p.Arg430=
|
|
NR_051961.2:n.1372C=
|
|
|
NM_001267554.2:c.1102C=
|
NP_001254483.1:p.Arg368=
|
|