|
NM_014026.6:c.550G>A
MANE Select
|
NP_054745.1:p.Ala184Thr
|
|
ENST00000263579.5:c.550G>A
MANE Select
|
ENSP00000263579.4:p.Ala184Thr
|
|
NM_001350236.1:c.571G>A
|
NP_001337165.1:p.Ala191Thr
|
|
NM_001350236.2:c.571G>A
|
NP_001337165.1:p.Ala191Thr
|
|
NM_014026.4:c.550G>A
|
NP_054745.1:p.Ala184Thr
|
|
NM_014026.5:c.550G>A
|
NP_054745.1:p.Ala184Thr
|
|
ENST00000263579.4:c.550G>A
|
ENSP00000263579.4:p.Ala184Thr
|
|
ENST00000529149.1:n.1900G>A
|
|
|
ENST00000530860.5:n.148-4994G>A
|
|
|
ENST00000648516.1:c.271G>A
|
ENSP00000497684.1:p.Ala91Thr
|
|
XM_011542778.1:c.571G>A
|
XP_011541080.1:p.Ala191Thr
|
|
XM_011542779.1:c.271G>A
|
XP_011541081.1:p.Ala91Thr
|
|
XM_011542780.1:c.271G>A
|
XP_011541082.1:p.Ala91Thr
|