ENST00000342741.6:c.814C=
MANE Select
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ENSP00000339933.4:p.Leu272=
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ENST00000342741.4:c.814C=
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ENSP00000339933.4:p.Leu272=
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|
ENST00000392414.7:c.721C=
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ENSP00000376214.3:p.Leu241=
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NM_000298.5:c.814C=
|
NP_000289.1:p.Leu272=
|
|
NM_181871.3:c.721C=
|
NP_870986.1:p.Leu241=
|
|
XM_005245266.3:c.973C=
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XP_005245323.1:p.Leu325=
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XM_006711386.2:c.622C=
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XP_006711449.1:p.Leu208=
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|
XM_011509639.1:c.973C=
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XP_011507941.1:p.Leu325=
|
|
XM_011509640.1:c.622C=
|
XP_011507942.1:p.Leu208=
|
|
NM_000298.6:c.814C=
MANE Select
|
NP_000289.1:p.Leu272=
|
|
XM_006711386.4:c.622C=
|
XP_006711449.1:p.Leu208=
|
|
XM_011509640.3:c.622C=
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XP_011507942.1:p.Leu208=
|
|
XM_017001493.1:c.814C=
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XP_016856982.1:p.Leu272=
|
|
NM_181871.4:c.721C=
|
NP_870986.1:p.Leu241=
|
|