ENST00000255531.8:c.2660T>C
|
ENSP00000255531.7:p.Val887Ala
|
|
ENST00000373034.8:c.2801T>C
MANE Select
|
ENSP00000362125.4:p.Val934Ala
|
|
ENST00000420881.6:c.2657T>C
|
ENSP00000400327.2:p.Val886Ala
|
|
NM_001105243.1:c.2660T>C
|
NP_001098713.1:p.Val887Ala
|
|
NM_001184880.1:c.2801T>C
|
NP_001171809.1:p.Val934Ala
|
|
NM_020766.2:c.2657T>C
|
NP_065817.2:p.Val886Ala
|
|
XM_011530997.1:c.2798T>C
|
XP_011529299.1:p.Val933Ala
|
|
XM_011530997.2:c.2798T>C
|
XP_011529299.1:p.Val933Ala
|
|
NM_001105243.2:c.2660T>C
|
NP_001098713.1:p.Val887Ala
|
|
NM_001184880.2:c.2801T>C
MANE Select
|
NP_001171809.1:p.Val934Ala
|
|
NM_020766.3:c.2657T>C
|
NP_065817.2:p.Val886Ala
|
|