ENST00000322776.11:c.1028T>G
MANE Select
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ENSP00000322450.6:p.Val343Gly
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ENST00000647561.1:c.1028T>G
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ENSP00000497587.1:p.Val343Gly
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ENST00000322776.10:c.1028T>G
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ENSP00000322450.6:p.Val343Gly
|
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ENST00000415352.6:c.1007T>G
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ENSP00000395368.2:p.Val336Gly
|
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ENST00000526169.1:n.656-5T>G
|
|
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ENST00000526770.5:n.1311T>G
|
|
|
ENST00000527355.5:c.317T>G
|
ENSP00000432637.1:p.Val106Gly
|
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ENST00000527923.1:n.370T>G
|
|
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ENST00000529927.5:c.1001T>G
|
ENSP00000436766.1:p.Val334Gly
|
|
ENST00000532303.5:c.725T>G
|
ENSP00000432015.1:p.Val242Gly
|
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ENST00000533919.5:c.432T>G
|
ENSP00000435199.1:n.432T>G
|
|
NM_001166102.1:c.1001T>G
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NP_001159574.1:p.Val334Gly
|
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NM_007103.3:c.1028T>G
|
NP_009034.2:p.Val343Gly
|
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NM_001166102.2:c.1001T>G
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NP_001159574.1:p.Val334Gly
|
|
NM_007103.4:c.1028T>G
MANE Select
|
NP_009034.2:p.Val343Gly
|
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