ENST00000541682.7:c.*37G>T
MANE Select
|
ENSP00000446205.2:n.*37G>T
|
|
ENST00000541682.6:c.730G>T
|
ENSP00000446205.2:n.730G>T
|
|
NM_001165967.1:c.*37G>T
|
NP_001159439.1:n.*37G>T
|
|
NM_032580.3:c.*37G>T
|
NP_115969.2:n.*37G>T
|
|
XM_011524038.1:c.*37G>T
|
XP_011522340.1:n.*37G>T
|
|
XM_011524039.1:c.*37G>T
|
XP_011522341.1:n.*37G>T
|
|
XM_011524040.1:c.*37G>T
|
XP_011522342.1:n.*37G>T
|
|
XM_011524041.1:c.*37G>T
|
XP_011522343.1:n.*37G>T
|
|
XM_011524042.1:c.*37G>T
|
XP_011522344.1:n.*37G>T
|
|
XR_934203.1:n.69+1720C>A
|
|
|
XM_017025232.1:c.*37G>T
|
XP_016880721.1:n.*37G>T
|
|
XM_024451007.1:c.*37G>T
|
XP_024306775.1:n.*37G>T
|
|
NM_001165967.2:c.*37G>T
MANE Select
|
NP_001159439.1:n.*37G>T
|
|
NM_032580.4:c.*37G>T
|
NP_115969.2:n.*37G>T
|
|