ENST00000695850.1:n.1002T>C
|
|
|
ENST00000695851.1:n.206T>C
|
|
|
ENST00000695853.1:c.*885T>C
|
ENSP00000512218.1:n.*885T>C
|
|
ENST00000423902.7:c.7826T>C
MANE Select
|
ENSP00000392028.1:p.Val2609Ala
|
|
ENST00000423902.6:c.7826T>C
|
ENSP00000392028.1:p.Val2609Ala
|
|
ENST00000524602.5:c.1717-1108T>C
|
ENSP00000437061.1:n.1717-1108T>C
|
|
ENST00000531695.1:n.250T>C
|
|
|
ENST00000618450.1:n.218T>C
|
|
|
NM_001316690.1:c.1717-1108T>C
|
NP_001303619.1:n.1717-1108T>C
|
|
NM_017780.3:c.7826T>C
|
NP_060250.2:p.Val2609Ala
|
|
XM_011517553.1:c.7916T>C
|
XP_011515855.1:p.Val2639Ala
|
|
XM_011517554.1:c.7916T>C
|
XP_011515856.1:p.Val2639Ala
|
|
XM_011517555.1:c.7913T>C
|
XP_011515857.1:p.Val2638Ala
|
|
XM_011517556.1:c.7699-1075T>C
|
XP_011515858.1:n.7699-1075T>C
|
|
XM_011517557.1:c.5903T>C
|
XP_011515859.1:p.Val1968Ala
|
|
XM_011517558.1:c.5453T>C
|
XP_011515860.1:p.Val1818Ala
|
|
XM_011517559.1:c.4661T>C
|
XP_011515861.1:p.Val1554Ala
|
|
XM_011517553.2:c.7916T>C
|
XP_011515855.1:p.Val2639Ala
|
|
XM_011517554.3:c.7916T>C
|
XP_011515856.1:p.Val2639Ala
|
|
XM_011517555.2:c.7913T>C
|
XP_011515857.1:p.Val2638Ala
|
|
XM_017013612.1:c.7916T>C
|
XP_016869101.1:p.Val2639Ala
|
|
XM_017013613.1:c.7823T>C
|
XP_016869102.1:p.Val2608Ala
|
|
NM_017780.4:c.7826T>C
MANE Select
|
NP_060250.2:p.Val2609Ala
|
|