ENST00000265517.10:c.387T>G
MANE Select
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ENSP00000265517.5:p.His129Gln
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ENST00000457717.6:c.387T>G
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ENSP00000400821.1:p.His129Gln
|
|
ENST00000511045.6:c.138T>G
|
ENSP00000427679.2:p.His46Gln
|
|
ENST00000265517.9:c.387T>G
|
ENSP00000265517.5:p.His129Gln
|
|
ENST00000422897.6:c.387T>G
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ENSP00000407350.2:p.His129Gln
|
|
ENST00000457717.5:c.387T>G
|
ENSP00000400821.1:p.His129Gln
|
|
ENST00000506883.5:c.417T>G
|
ENSP00000426755.1:p.His139Gln
|
|
ENST00000511045.5:c.468T>G
|
ENSP00000427679.1:p.His156Gln
|
|
ENST00000619629.1:c.387T>G
|
ENSP00000482850.1:p.His129Gln
|
|
NM_000253.3:c.387T>G
|
NP_000244.2:p.His129Gln
|
|
NM_001300785.1:c.468T>G
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NP_001287714.1:p.His156Gln
|
|
NM_000253.4:c.387T>G
|
NP_000244.2:p.His129Gln
|
|
NM_001300785.2:c.138T>G
|
NP_001287714.2:p.His46Gln
|
|
NM_001386140.1:c.387T>G
MANE Select
|
NP_001373069.1:p.His129Gln
|
|