ENST00000542639.6:c.496C>G
|
ENSP00000440846.1:p.Pro166Ala
|
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ENST00000686683.1:c.205C>G
|
ENSP00000509063.1:p.Pro69Ala
|
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ENST00000686980.1:n.1027C>G
|
|
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ENST00000688006.1:c.496C>G
|
ENSP00000510311.1:p.Pro166Ala
|
|
ENST00000688859.1:n.451C>G
|
|
|
ENST00000689087.1:c.496C>G
|
ENSP00000508997.1:p.Pro166Ala
|
|
ENST00000693128.1:c.790C>G
|
ENSP00000508493.1:p.Pro264Ala
|
|
ENST00000338702.4:c.895C>G
MANE Select
|
ENSP00000340684.3:p.Pro299Ala
|
|
ENST00000338702.3:c.895C>G
|
ENSP00000340684.3:p.Pro299Ala
|
|
ENST00000542639.5:c.496C>G
|
ENSP00000440846.1:p.Pro166Ala
|
|
NM_000240.3:c.895C>G
|
NP_000231.1:p.Pro299Ala
|
|
NM_001270458.1:c.496C>G
|
NP_001257387.1:p.Pro166Ala
|
|
NM_000240.4:c.895C>G
MANE Select
|
NP_000231.1:p.Pro299Ala
|
|
NM_001270458.2:c.496C>G
|
NP_001257387.1:p.Pro166Ala
|
|