ENST00000319397.7:c.*3297G>A
|
ENSP00000324578.5:n.*3297G>A
|
|
ENST00000392668.8:c.*3297G>A
MANE Select
|
ENSP00000376436.3:n.*3297G>A
|
|
ENST00000535549.5:c.*3297G>A
|
ENSP00000441430.1:n.*3297G>A
|
|
NM_001143820.1:c.*3297G>A
|
NP_001137292.1:n.*3297G>A
|
|
NM_001162422.1:c.*3297G>A
|
NP_001155894.1:n.*3297G>A
|
|
NM_005238.3:c.*3297G>A
|
NP_005229.1:n.*3297G>A
|
|
XM_011542649.1:c.*3297G>A
|
XP_011540951.1:n.*3297G>A
|
|
XM_011542650.1:c.*3297G>A
|
XP_011540952.1:n.*3297G>A
|
|
XM_011542651.1:c.*3297G>A
|
XP_011540953.1:n.*3297G>A
|
|
XM_011542652.1:c.*3297G>A
|
XP_011540954.1:n.*3297G>A
|
|
XR_948164.1:n.7784C>T
|
|
|
XR_948165.1:n.5035C>T
|
|
|
NM_001330451.1:c.*3297G>A
|
NP_001317380.1:n.*3297G>A
|
|
XM_017017314.1:c.*3297G>A
|
XP_016872803.1:n.*3297G>A
|
|
XM_017017317.1:c.*3297G>A
|
XP_016872806.1:n.*3297G>A
|
|
NM_001143820.2:c.*3297G>A
MANE Select
|
NP_001137292.1:n.*3297G>A
|
|
NM_001330451.2:c.*3297G>A
|
NP_001317380.1:n.*3297G>A
|
|
NM_005238.4:c.*3297G>A
|
NP_005229.1:n.*3297G>A
|
|
NM_001162422.2:c.*3297G>A
|
NP_001155894.1:n.*3297G>A
|
|