ENST00000281928.9:c.5939T>C
MANE Select
|
ENSP00000281928.3:p.Met1980Thr
|
|
ENST00000548784.2:n.2153T>C
|
|
|
ENST00000648379.1:n.4307T>C
|
|
|
ENST00000648737.1:n.5703T>C
|
|
|
ENST00000648825.1:n.4124T>C
|
|
|
ENST00000648916.1:n.3950T>C
|
|
|
ENST00000649607.1:c.4123T>C
|
|
|
ENST00000649775.1:c.2428T>C
|
|
|
ENST00000650226.1:c.5975T>C
|
ENSP00000496981.1:p.Met1992Thr
|
|
ENST00000281928.7:c.5939T>C
|
ENSP00000281928.3:p.Met1980Thr
|
|
ENST00000548784.1:n.437T>C
|
|
|
ENST00000552447.1:c.552T>C
|
|
|
NM_015335.4:c.5939T>C
|
NP_056150.1:p.Met1980Thr
|
|
XM_011538080.1:c.5975T>C
|
XP_011536382.1:p.Met1992Thr
|
|
XM_011538081.1:c.5972T>C
|
XP_011536383.1:p.Met1991Thr
|
|
XM_011538082.1:c.5945T>C
|
XP_011536384.1:p.Met1982Thr
|
|
XM_011538080.2:c.5975T>C
|
XP_011536382.1:p.Met1992Thr
|
|
XM_011538081.2:c.5972T>C
|
XP_011536383.1:p.Met1991Thr
|
|
XM_011538082.2:c.5945T>C
|
XP_011536384.1:p.Met1982Thr
|
|
XM_017019090.1:c.5936T>C
|
XP_016874579.1:p.Met1979Thr
|
|
NM_015335.5:c.5939T>C
MANE Select
|
NP_056150.1:p.Met1980Thr
|
|