ENST00000614565.5:c.1936C>G
MANE Select
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ENSP00000484928.1:p.Pro646Ala
|
|
ENST00000543233.2:c.1714C>G
|
ENSP00000443301.1:p.Pro572Ala
|
|
ENST00000611855.4:c.1654C>G
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ENSP00000480844.1:p.Pro552Ala
|
|
ENST00000614565.4:c.1936C>G
|
ENSP00000484928.1:p.Pro646Ala
|
|
NM_001252338.2:c.1825C>G
|
NP_001239267.1:p.Pro609Ala
|
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NM_001252339.2:c.1714C>G
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NP_001239268.1:p.Pro572Ala
|
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NM_001794.4:c.1936C>G
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NP_001785.2:p.Pro646Ala
|
|
NM_001794.5:c.1936C>G
MANE Select
|
NP_001785.2:p.Pro646Ala
|
|
NM_001252339.3:c.1714C>G
|
NP_001239268.1:p.Pro572Ala
|
|