ENST00000369689.6:c.294T>C
MANE Select
|
ENSP00000358703.1:p.Ala98=
|
|
ENST00000369687.2:c.120T>C
|
ENSP00000358701.1:p.Ala40=
|
|
ENST00000369689.5:c.294T>C
|
ENSP00000358703.1:p.Ala98=
|
|
ENST00000635617.1:n.3707T>C
|
|
|
NM_001009994.2:c.294T>C
|
NP_001009994.1:p.Ala98=
|
|
NR_103525.1:n.351T>C
|
|
|
NR_103525.2:n.289T>C
|
|
|
NM_001009994.3:c.294T>C
MANE Select
|
NP_001009994.1:p.Ala98=
|
|
NM_001400774.1:c.-28+3135T>C
|
NP_001387703.1:n.-28+3135T>C
|
|
NM_001400899.1:c.357T>C
|
NP_001387828.1:p.Ala119=
|
|
NM_001400900.1:c.*3131T>C
|
NP_001387829.1:n.*3131T>C
|
|
NR_174603.1:n.234+3135T>C
|
|
|
NR_174604.1:n.296+3135T>C
|
|
|
NR_174605.1:n.455+3237T>C
|
|
|
NR_174622.1:n.3369T>C
|
|
|