ENST00000271751.10:c.1482C>T
MANE Select
|
ENSP00000271751.4:p.Ile494=
|
|
ENST00000367007.5:c.1401C>T
|
ENSP00000355974.5:p.Ile467=
|
|
ENST00000638357.1:c.815C>T
|
|
|
ENST00000638498.1:c.1482C>T
|
ENSP00000490983.1:p.Ile494=
|
|
ENST00000638960.1:c.1401C>T
|
ENSP00000492302.1:p.Ile467=
|
|
ENST00000639952.1:c.1401C>T
|
ENSP00000492697.1:p.Ile467=
|
|
ENST00000640044.1:c.330C>T
|
ENSP00000491434.1:p.Ile110=
|
|
ENST00000640243.1:c.971C>T
|
ENSP00000492803.1:p.Ser324Phe
|
|
ENST00000640522.1:c.1052C>T
|
ENSP00000491019.1:p.Ser351Phe
|
|
ENST00000640528.1:c.1401C>T
|
ENSP00000491725.1:p.Ile467=
|
|
ENST00000640566.1:c.311-28603C>T
|
ENSP00000491302.1:n.311-28603C>T
|
|
ENST00000640710.1:c.1401C>T
|
ENSP00000492513.1:p.Ile467=
|
|
ENST00000271751.8:c.1482C>T
|
ENSP00000271751.4:p.Ile494=
|
|
ENST00000367007.4:c.1401C>T
|
ENSP00000355974.4:p.Ile467=
|
|
NM_002238.3:c.1401C>T
|
NP_002229.1:p.Ile467=
|
|
NM_172362.2:c.1482C>T
|
NP_758872.1:p.Ile494=
|
|
XM_011509514.1:c.306C>T
|
XP_011507816.1:p.Ile102=
|
|
XM_017001246.1:c.306C>T
|
XP_016856735.1:p.Ile102=
|
|
NM_172362.3:c.1482C>T
MANE Select
|
NP_758872.1:p.Ile494=
|
|
NM_002238.4:c.1401C>T
|
NP_002229.1:p.Ile467=
|
|