NM_005921.2:c.4257+290G>C
MANE Select
|
NP_005912.1:n.4257+290G>C
|
ENST00000399503.4:c.4257+290G>C
MANE Select
|
ENSP00000382423.3:n.4257+290G>C
|
NM_005921.1:c.4257+290G>C
|
NP_005912.1:n.4257+290G>C
|
ENST00000399503.3:c.4257+290G>C
|
ENSP00000382423.3:n.4257+290G>C
|
ENST00000469188.1:n.544G>C
|
|
XM_005248519.3:c.3879+290G>C
|
XP_005248576.2:n.3879+290G>C
|
XM_011543406.1:c.4002+290G>C
|
XP_011541708.1:n.4002+290G>C
|
XM_011543407.1:c.3978+290G>C
|
XP_011541709.1:n.3978+290G>C
|
XM_011543408.1:c.4115-416G>C
|
XP_011541710.1:n.4115-416G>C
|
XM_017009484.1:c.3846+290G>C
|
XP_016864973.1:n.3846+290G>C
|
XM_017009485.1:c.3768+290G>C
|
XP_016864974.1:n.3768+290G>C
|
XR_001742068.2:n.4146-416G>C
|
|