ENST00000299314.12:c.3219A>T
MANE Select
|
ENSP00000299314.7:p.Pro1073=
|
|
ENST00000299314.11:c.3219A>T
|
ENSP00000299314.7:p.Pro1073=
|
|
ENST00000549194.1:n.85A>T
|
|
|
ENST00000550718.1:c.31A>T
|
|
|
NM_024312.4:c.3219A>T
|
NP_077288.2:p.Pro1073=
|
|
XM_006719593.2:c.3219A>T
|
XP_006719656.1:p.Pro1073=
|
|
XM_011538731.1:c.3138A>T
|
XP_011537033.1:p.Pro1046=
|
|
XM_006719593.3:c.3219A>T
|
XP_006719656.1:p.Pro1073=
|
|
XM_011538731.2:c.3138A>T
|
XP_011537033.1:p.Pro1046=
|
|
XM_017019961.1:c.3003A>T
|
XP_016875450.1:p.Pro1001=
|
|
XM_017019962.2:c.1992A>T
|
XP_016875451.1:p.Pro664=
|
|
NM_024312.5:c.3219A>T
MANE Select
|
NP_077288.2:p.Pro1073=
|
|