ENST00000593677.2:c.839G=
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|
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ENST00000688602.1:c.2236G=
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|
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ENST00000689936.1:c.2208G=
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|
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ENST00000359596.8:c.13903G=
MANE Select
|
ENSP00000352608.2:p.Glu4635=
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ENST00000355481.8:c.13888G=
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ENSP00000347667.3:p.Glu4630=
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ENST00000359596.7:c.13903G=
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ENSP00000352608.2:p.Glu4635=
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|
ENST00000360985.7:c.13885G=
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ENSP00000354254.4:p.Glu4629=
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ENST00000593677.1:c.363G=
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|
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NM_000540.2:c.13903G= , LRG_766t1:c.13903G=
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NP_000531.2:p.Glu4635=
|
|
NM_001042723.1:c.13888G=
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NP_001036188.1:p.Glu4630=
|
|
XM_006723317.1:c.13885G=
|
XP_006723380.1:p.Glu4629=
|
|
XM_006723319.1:c.13870G=
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XP_006723382.1:p.Glu4624=
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XM_011527204.1:c.13900G=
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XP_011525506.1:p.Glu4634=
|
|
XM_011527205.1:c.13816G=
|
XP_011525507.1:p.Glu4606=
|
|
XM_006723317.2:c.13885G=
|
XP_006723380.1:p.Glu4629=
|
|
XM_006723319.2:c.13870G=
|
XP_006723382.1:p.Glu4624=
|
|
XM_011527205.2:c.13816G=
|
XP_011525507.1:p.Glu4606=
|
|
NM_000540.3:c.13903G=
MANE Select
|
NP_000531.2:p.Glu4635=
|
|
NM_001042723.2:c.13888G=
|
NP_001036188.1:p.Glu4630=
|
|