ENST00000692443.1:c.302T>G
MANE Select
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ENSP00000509163.1:p.Leu101Trp
|
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ENST00000419277.5:c.302T>G
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ENSP00000393566.1:p.Leu101Trp
|
|
ENST00000453337.1:c.302T>G
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ENSP00000390929.1:p.Leu101Trp
|
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ENST00000463066.1:n.397T>G
|
|
|
ENST00000476642.5:n.278T>G
|
|
|
ENST00000479107.1:n.347T>G
|
|
|
NM_001242524.1:c.302T>G
|
NP_001229453.1:p.Leu101Trp
|
|
NM_001242525.1:c.302T>G
|
NP_001229454.1:p.Leu101Trp
|
|
NM_033554.3:c.302T>G
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NP_291032.2:p.Leu101Trp
|
|
XM_011514559.1:c.302T>G
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XP_011512861.1:p.Leu101Trp
|
|
NM_001242524.2:c.302T>G
|
NP_001229453.1:p.Leu101Trp
|
|
NM_001242525.2:c.302T>G
|
NP_001229454.1:p.Leu101Trp
|
|