ENST00000649448.1:c.833T>C
|
ENSP00000497165.1:p.Met278Thr
|
|
ENST00000650372.1:c.2516T>C
MANE Select
|
ENSP00000497931.1:p.Met839Thr
|
|
ENST00000263817.6:c.2516T>C
|
ENSP00000263817.6:p.Met839Thr
|
|
ENST00000439188.1:c.1205T>C
|
ENSP00000416058.1:n.1205T>C
|
|
NM_003742.2:c.2516T>C
|
NP_003733.2:p.Met839Thr
|
|
XM_006712817.2:c.2558T>C
|
XP_006712880.1:p.Met853Thr
|
|
XM_011512077.1:c.2618T>C
|
XP_011510379.1:p.Met873Thr
|
|
XM_011512078.1:c.2618T>C
|
XP_011510380.1:p.Met873Thr
|
|
XM_011512079.1:c.2618T>C
|
XP_011510381.1:p.Met873Thr
|
|
XM_011512080.1:c.2618T>C
|
XP_011510382.1:p.Met873Thr
|
|
XM_011512081.1:c.842T>C
|
XP_011510383.1:p.Met281Thr
|
|
NM_003742.4:c.2516T>C
MANE Select
|
NP_003733.2:p.Met839Thr
|
|
XM_006712817.3:c.2558T>C
|
XP_006712880.1:p.Met853Thr
|
|
XM_011512077.2:c.2618T>C
|
XP_011510379.1:p.Met873Thr
|
|
XM_011512078.2:c.2618T>C
|
XP_011510380.1:p.Met873Thr
|
|
XM_011512080.2:c.2618T>C
|
XP_011510382.1:p.Met873Thr
|
|
XM_011512081.2:c.842T>C
|
XP_011510383.1:p.Met281Thr
|
|
XM_017005165.1:c.2618T>C
|
XP_016860654.1:p.Met873Thr
|
|
XM_017005166.1:c.1847T>C
|
XP_016860655.1:p.Met616Thr
|
|
XM_017005167.1:c.1301T>C
|
XP_016860656.1:p.Met434Thr
|
|