ENST00000256084.8:c.2990G=
MANE Select
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ENSP00000256084.7:p.Arg997=
|
|
ENST00000256084.7:c.2990G=
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ENSP00000256084.7:p.Arg997=
|
|
ENST00000359874.7:c.3080G=
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ENSP00000352936.3:p.Arg1027=
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|
NM_001127698.1:c.3080G=
|
NP_001121170.1:p.Arg1027=
|
|
NM_006846.3:c.2990G= , LRG_110t1:c.2990G=
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NP_006837.2:p.Arg997=
|
|
XM_011537550.1:c.3023G=
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XP_011535852.1:p.Arg1008=
|
|
XM_011537551.1:c.2996G=
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XP_011535853.1:p.Arg999=
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|
XM_011537551.2:c.2996G=
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XP_011535853.1:p.Arg999=
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|
NM_001127698.2:c.3080G=
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NP_001121170.1:p.Arg1027=
|
|
NM_006846.4:c.2990G=
MANE Select
|
NP_006837.2:p.Arg997=
|
|