ENST00000359595.8:c.140T>C
MANE Select
|
ENSP00000352606.4:p.Val47Ala
|
|
ENST00000359595.7:c.140T>C
|
ENSP00000352606.3:p.Val47Ala
|
|
ENST00000558770.5:c.140T>C
|
ENSP00000456458.1:p.Val47Ala
|
|
ENST00000562281.1:c.140T>C
|
ENSP00000456985.1:p.Val47Ala
|
|
ENST00000562889.5:c.326T>C
|
ENSP00000457180.1:p.Val109Ala
|
|
ENST00000563808.1:n.242T>C
|
|
|
NM_001307952.1:c.326T>C
|
NP_001294881.1:p.Val109Ala
|
|
NM_178232.2:c.140T>C
|
NP_839946.1:p.Val47Ala
|
|
NM_178232.3:c.140T>C
|
NP_839946.1:p.Val47Ala
|
|
XM_011521261.1:c.272T>C
|
XP_011519563.1:p.Val91Ala
|
|
XR_243204.1:n.355T>C
|
|
|
XR_931756.1:n.461T>C
|
|
|
XM_017021934.2:c.326T>C
|
XP_016877423.1:p.Val109Ala
|
|
XM_017021935.2:c.-240T>C
|
XP_016877424.1:n.-240T>C
|
|
XM_017021936.2:c.-240T>C
|
XP_016877425.1:n.-240T>C
|
|
XR_001751098.2:n.473T>C
|
|
|
XR_931756.3:n.474T>C
|
|
|
NM_001307952.2:c.326T>C
|
NP_001294881.1:p.Val109Ala
|
|
NM_178232.4:c.140T>C
MANE Select
|
NP_839946.1:p.Val47Ala
|
|