ENST00000688602.1:c.1225C>G
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|
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ENST00000689936.1:c.1207C>G
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|
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ENST00000359596.8:c.12815C>G
MANE Select
|
ENSP00000352608.2:p.Ala4272Gly
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ENST00000355481.8:c.12800C>G
|
ENSP00000347667.3:p.Ala4267Gly
|
|
ENST00000359596.7:c.12815C>G
|
ENSP00000352608.2:p.Ala4272Gly
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ENST00000360985.7:c.12797C>G
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ENSP00000354254.4:p.Ala4266Gly
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ENST00000594335.5:c.6184C>G
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NM_000540.2:c.12815C>G , LRG_766t1:c.12815C>G
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NP_000531.2:p.Ala4272Gly
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NM_001042723.1:c.12800C>G
|
NP_001036188.1:p.Ala4267Gly
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XM_006723317.1:c.12797C>G
|
XP_006723380.1:p.Ala4266Gly
|
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XM_006723319.1:c.12782C>G
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XP_006723382.1:p.Ala4261Gly
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XM_011527204.1:c.12812C>G
|
XP_011525506.1:p.Ala4271Gly
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|
XM_011527205.1:c.12815C>G
|
XP_011525507.1:p.Ala4272Gly
|
|
XM_006723317.2:c.12797C>G
|
XP_006723380.1:p.Ala4266Gly
|
|
XM_006723319.2:c.12782C>G
|
XP_006723382.1:p.Ala4261Gly
|
|
XM_011527205.2:c.12815C>G
|
XP_011525507.1:p.Ala4272Gly
|
|
NM_000540.3:c.12815C>G
MANE Select
|
NP_000531.2:p.Ala4272Gly
|
|
NM_001042723.2:c.12800C>G
|
NP_001036188.1:p.Ala4267Gly
|
|