ENST00000342741.6:c.1481T=
MANE Select
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ENSP00000339933.4:p.Ile494=
|
|
ENST00000342741.4:c.1481T=
|
ENSP00000339933.4:p.Ile494=
|
|
ENST00000392414.7:c.1388T=
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ENSP00000376214.3:p.Ile463=
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|
NM_000298.5:c.1481T=
|
NP_000289.1:p.Ile494=
|
|
NM_181871.3:c.1388T=
|
NP_870986.1:p.Ile463=
|
|
XM_005245266.3:c.1640T=
|
XP_005245323.1:p.Ile547=
|
|
XM_006711386.2:c.1289T=
|
XP_006711449.1:p.Ile430=
|
|
XM_011509640.1:c.1289T=
|
XP_011507942.1:p.Ile430=
|
|
NM_000298.6:c.1481T=
MANE Select
|
NP_000289.1:p.Ile494=
|
|
XM_006711386.4:c.1289T=
|
XP_006711449.1:p.Ile430=
|
|
XM_011509640.3:c.1289T=
|
XP_011507942.1:p.Ile430=
|
|
NM_181871.4:c.1388T=
|
NP_870986.1:p.Ile463=
|
|