ENST00000309383.6:c.2090-658T>C
MANE Select
|
ENSP00000310649.1:n.2090-658T>C
|
|
ENST00000309383.5:c.2090-658T>C
|
ENSP00000310649.1:n.2090-658T>C
|
|
ENST00000326848.7:c.1175-658T>C
|
ENSP00000320853.7:n.1175-658T>C
|
|
ENST00000590333.5:c.2138-658T>C
|
ENSP00000468190.1:n.2138-658T>C
|
|
NM_032430.1:c.2090-658T>C
|
NP_115806.1:n.2090-658T>C
|
|
XM_005259327.2:c.1820-658T>C
|
XP_005259384.1:n.1820-658T>C
|
|
XM_011527395.1:c.1847-658T>C
|
XP_011525697.1:n.1847-658T>C
|
|
XR_430213.2:n.2073-658T>C
|
|
|
XM_005259327.3:c.1820-658T>C
|
XP_005259384.1:n.1820-658T>C
|
|
XM_011527395.2:c.1562-658T>C
|
XP_011525697.2:n.1562-658T>C
|
|
XM_024451739.1:c.1865-658T>C
|
XP_024307507.1:n.1865-658T>C
|
|
XR_430213.4:n.2371-658T>C
|
|
|
NM_032430.2:c.2090-658T>C
MANE Select
|
NP_115806.1:n.2090-658T>C
|
|