ENST00000297784.10:c.1862T>C
MANE Select
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ENSP00000297784.6:p.Val621Ala
|
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ENST00000644967.1:c.*302T>C
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ENSP00000496159.1:n.*302T>C
|
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ENST00000645053.1:c.1258-5929T>C
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ENSP00000493838.1:n.1258-5929T>C
|
|
ENST00000645208.2:c.1862T>C
|
ENSP00000494684.1:p.Val621Ala
|
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ENST00000645773.1:c.1736T>C
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ENSP00000493698.1:p.Val579Ala
|
|
ENST00000645787.1:n.2005T>C
|
|
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ENST00000646619.1:c.1424T>C
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ENSP00000493726.1:p.Val475Ala
|
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ENST00000651183.1:c.1424T>C
|
ENSP00000498723.1:p.Val475Ala
|
|
ENST00000297784.9:c.1862T>C
|
ENSP00000297784.5:p.Val621Ala
|
|
ENST00000340019.4:c.1862T>C
|
ENSP00000341433.3:p.Val621Ala
|
|
ENST00000469455.1:n.343T>C
|
|
|
ENST00000486417.5:n.760T>C
|
|
|
NM_138691.2:c.1862T>C
|
NP_619636.2:p.Val621Ala
|
|
XM_011518213.1:c.2450T>C
|
XP_011516515.1:p.Val817Ala
|
|
XM_017014256.1:c.1865T>C
|
XP_016869745.1:p.Val622Ala
|
|
NM_138691.3:c.1862T>C
MANE Select
|
NP_619636.2:p.Val621Ala
|
|