ENST00000369689.6:c.268G>T
MANE Select
|
ENSP00000358703.1:p.Asp90Tyr
|
|
ENST00000369687.2:c.94G>T
|
ENSP00000358701.1:p.Asp32Tyr
|
|
ENST00000369689.5:c.268G>T
|
ENSP00000358703.1:p.Asp90Tyr
|
|
ENST00000635617.1:n.3681G>T
|
|
|
NM_001009994.2:c.268G>T
|
NP_001009994.1:p.Asp90Tyr
|
|
NR_103525.1:n.325G>T
|
|
|
NR_103525.2:n.263G>T
|
|
|
NM_001009994.3:c.268G>T
MANE Select
|
NP_001009994.1:p.Asp90Tyr
|
|
NM_001400774.1:c.-28+3109G>T
|
NP_001387703.1:n.-28+3109G>T
|
|
NM_001400899.1:c.331G>T
|
NP_001387828.1:p.Asp111Tyr
|
|
NM_001400900.1:c.*3105G>T
|
NP_001387829.1:n.*3105G>T
|
|
NR_174603.1:n.234+3109G>T
|
|
|
NR_174604.1:n.296+3109G>T
|
|
|
NR_174605.1:n.455+3211G>T
|
|
|
NR_174622.1:n.3343G>T
|
|
|