|
NM_005921.2:c.1035+12C>T
MANE Select
|
NP_005912.1:n.1035+12C>T
|
|
ENST00000399503.4:c.1035+12C>T
MANE Select
|
ENSP00000382423.3:n.1035+12C>T
|
|
NM_005921.1:c.1035+12C>T
|
NP_005912.1:n.1035+12C>T
|
|
ENST00000399503.3:c.1035+12C>T
|
ENSP00000382423.3:n.1035+12C>T
|
|
XM_005248519.3:c.657+12C>T
|
XP_005248576.2:n.657+12C>T
|
|
XM_011543406.1:c.780+12C>T
|
XP_011541708.1:n.780+12C>T
|
|
XM_011543407.1:c.1035+12C>T
|
XP_011541709.1:n.1035+12C>T
|
|
XM_011543408.1:c.1035+12C>T
|
XP_011541710.1:n.1035+12C>T
|
|
XM_017009484.1:c.624+12C>T
|
XP_016864973.1:n.624+12C>T
|
|
XM_017009485.1:c.546+12C>T
|
XP_016864974.1:n.546+12C>T
|
|
XR_001742068.2:n.1066+12C>T
|
|