ENST00000394009.5:c.*550C>T
(BBOF1)
MANE Select
|
ENSP00000377577.3:n.*550C>T
|
|
ENST00000553458.6:c.1336G>A
(ALDH6A1)
MANE Select
|
ENSP00000450436.1:p.Gly446Arg
|
|
ENST00000350259.8:c.1297G>A
(ALDH6A1)
|
ENSP00000342564.4:p.Gly433Arg
|
|
ENST00000394009.4:c.*550C>T
(BBOF1)
|
ENSP00000377577.3:n.*550C>T
|
|
ENST00000492026.4:n.1379+7991C>T
(BBOF1)
|
|
|
ENST00000553458.5:c.1336G>A
(ALDH6A1)
|
ENSP00000450436.1:p.Gly446Arg
|
|
ENST00000554501.5:n.1554G>A
(ALDH6A1)
|
|
|
ENST00000555126.1:c.487G>A
(ALDH6A1)
|
ENSP00000452081.1:p.Gly163Arg
|
|
NM_001278593.1:c.1297G>A
(ALDH6A1)
|
NP_001265522.1:p.Gly433Arg
|
|
NM_001278594.1:c.874G>A
(ALDH6A1)
|
NP_001265523.1:p.Gly292Arg
|
|
NM_005589.3:c.1336G>A
(ALDH6A1)
|
NP_005580.1:p.Gly446Arg
|
|
NM_025057.2:c.*550C>T
(BBOF1)
|
NP_079333.2:n.*550C>T
|
|
XM_011537172.1:c.1686+7991C>T
(BBOF1)
|
XP_011535474.1:n.1686+7991C>T
|
|
XM_011537173.1:c.1693+7984C>T
(BBOF1)
|
XP_011535475.1:n.1693+7984C>T
|
|
XM_011537174.1:c.*550C>T
(BBOF1)
|
XP_011535476.1:n.*550C>T
|
|
XM_011537171.2:c.*461C>T
(BBOF1)
|
XP_011535473.1:n.*461C>T
|
|
XM_011537174.2:c.*550C>T
(BBOF1)
|
XP_011535476.1:n.*550C>T
|
|
XM_017021331.2:c.874G>A
(ALDH6A1)
|
XP_016876820.1:p.Gly292Arg
|
|
XM_017021659.1:c.1578+7991C>T
(BBOF1)
|
XP_016877148.1:n.1578+7991C>T
|
|
XM_017021660.1:c.*461C>T
(BBOF1)
|
XP_016877149.1:n.*461C>T
|
|
XM_017021661.1:c.*550C>T
(BBOF1)
|
XP_016877150.1:n.*550C>T
|
|
XM_017021662.1:c.*550C>T
(BBOF1)
|
XP_016877151.1:n.*550C>T
|
|
XM_017021663.1:c.*550C>T
(BBOF1)
|
XP_016877152.1:n.*550C>T
|
|
NM_025057.3:c.*550C>T
(BBOF1)
MANE Select
|
NP_079333.2:n.*550C>T
|
|
NM_001278593.2:c.1297G>A
(ALDH6A1)
|
NP_001265522.1:p.Gly433Arg
|
|
NM_001278594.2:c.874G>A
(ALDH6A1)
|
NP_001265523.1:p.Gly292Arg
|
|
NM_005589.4:c.1336G>A
(ALDH6A1)
MANE Select
|
NP_005580.1:p.Gly446Arg
|
|