ENST00000650793.2:n.487T>C
|
|
|
ENST00000697612.1:n.1165T>C
|
|
|
ENST00000374881.3:c.296T>C
|
ENSP00000364015.2:p.Val99Ala
|
|
ENST00000374882.8:c.308T>C
MANE Select
|
ENSP00000364016.4:p.Val103Ala
|
|
ENST00000650411.1:n.1629T>C
|
|
|
ENST00000650793.1:n.487T>C
|
|
|
ENST00000374881.2:c.296T>C
|
ENSP00000364015.2:p.Val99Ala
|
|
ENST00000374882.7:c.308T>C
|
ENSP00000364016.3:p.Val103Ala
|
|
ENST00000395339.7:c.296-60T>C
|
ENSP00000378748.3:n.296-60T>C
|
|
ENST00000484003.1:n.692T>C
|
|
|
NM_004159.4:c.296T>C
|
NP_004150.1:p.Val99Ala
|
|
NM_148919.3:c.308T>C
|
NP_683720.2:p.Val103Ala
|
|
NM_148919.4:c.308T>C
MANE Select
|
NP_683720.2:p.Val103Ala
|
|
NM_004159.5:c.296T>C
|
NP_004150.1:p.Val99Ala
|
|