ENST00000346342.8:c.1104C>A
MANE Select
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ENSP00000329546.4:p.Ala368=
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ENST00000346342.7:c.1104C>A
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ENSP00000329546.3:p.Ala368=
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ENST00000375581.3:c.1170C>A
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ENSP00000364731.3:p.Ala390=
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ENST00000541084.5:c.918C>A
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ENSP00000442051.2:p.Ala306=
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NM_000131.4:c.1170C>A , LRG_554t1:c.1170C>A
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NP_000122.1:p.Ala390=
|
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NM_001267554.1:c.918C>A
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NP_001254483.1:p.Ala306=
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NM_019616.3:c.1104C>A , LRG_554t2:c.1104C>A
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NP_062562.1:p.Ala368=
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NR_051961.1:n.1191C>A
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|
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XM_006719963.2:c.963C>A
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XP_006720026.1:p.Ala321=
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XM_011537474.1:c.1212C>A
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XP_011535776.1:p.Ala404=
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XM_011537475.1:c.1026C>A
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XP_011535777.1:p.Ala342=
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XM_011537476.1:c.864C>A
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XP_011535778.1:p.Ala288=
|
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XM_011537477.1:c.1173C>A
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XP_011535779.1:p.Ala391=
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XM_006719963.3:c.1008C>A
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XP_006720026.2:p.Ala336=
|
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XM_011537474.2:c.1257C>A
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XP_011535776.2:p.Ala419=
|
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XM_011537475.2:c.1071C>A
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XP_011535777.2:p.Ala357=
|
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XM_011537476.2:c.864C>A
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XP_011535778.1:p.Ala288=
|
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NM_019616.4:c.1104C>A
MANE Select
|
NP_062562.1:p.Ala368=
|
|
NR_051961.2:n.1188C>A
|
|
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NM_001267554.2:c.918C>A
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NP_001254483.1:p.Ala306=
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