ENST00000252288.8:c.531G>A
MANE Select
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ENSP00000252288.1:p.Leu177=
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ENST00000447102.8:c.531G>A
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ENSP00000403536.2:p.Leu177=
|
|
ENST00000591788.3:c.214G>A
|
|
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ENST00000640164.1:n.364G>A
|
|
|
ENST00000640762.1:c.462G>A
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ENSP00000492031.1:p.Leu154=
|
|
ENST00000252288.6:c.531G>A
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ENSP00000252288.1:p.Leu177=
|
|
ENST00000447102.7:c.531G>A
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ENSP00000403536.2:p.Leu177=
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|
ENST00000591788.2:c.216G>A
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ENSP00000466341.2:p.Leu72=
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|
NM_000156.5:c.531G>A
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NP_000147.1:p.Leu177=
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|
NM_138924.2:c.531G>A
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NP_620279.1:p.Leu177=
|
|
NM_000156.6:c.531G>A
MANE Select
|
NP_000147.1:p.Leu177=
|
|
NM_138924.3:c.531G>A
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NP_620279.1:p.Leu177=
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