ENST00000302347.10:c.1241T>C
|
ENSP00000303242.6:p.Val414Ala
|
|
ENST00000652462.1:c.1169T>C
MANE Select
|
ENSP00000498780.1:p.Val390Ala
|
|
ENST00000302347.9:c.1169T>C
|
ENSP00000303242.5:p.Val390Ala
|
|
ENST00000355153.8:c.1169T>C
|
ENSP00000347279.4:p.Val390Ala
|
|
ENST00000397850.6:c.1169T>C
|
ENSP00000380948.2:p.Val390Ala
|
|
ENST00000397852.5:c.1169T>C
|
ENSP00000380950.1:p.Val390Ala
|
|
ENST00000397854.7:c.998T>C
|
ENSP00000380952.3:p.Val333Ala
|
|
ENST00000397857.5:c.1169T>C
|
ENSP00000380955.1:p.Val390Ala
|
|
ENST00000475170.5:n.569T>C
|
|
|
ENST00000498666.5:n.2738T>C
|
|
|
ENST00000523323.5:c.*996T>C
|
ENSP00000427732.1:n.*996T>C
|
|
ENST00000610622.4:c.998T>C
|
ENSP00000480700.1:p.Val333Ala
|
|
NM_000211.4:c.1169T>C
|
NP_000202.3:p.Val390Ala
|
|
NM_001127491.2:c.1169T>C
|
NP_001120963.2:p.Val390Ala
|
|
NM_001303238.1:c.962T>C
|
NP_001290167.1:p.Val321Ala
|
|
XM_006724001.1:c.962T>C
|
XP_006724064.1:p.Val321Ala
|
|
XM_006724001.2:c.962T>C
|
XP_006724064.1:p.Val321Ala
|
|
NM_000211.5:c.1169T>C
MANE Select
|
NP_000202.3:p.Val390Ala
|
|
NM_001127491.3:c.1169T>C
|
NP_001120963.2:p.Val390Ala
|
|
NM_001303238.2:c.962T>C
|
NP_001290167.1:p.Val321Ala
|
|