ENST00000237596.7:c.1094+269G>A
MANE Select
|
ENSP00000237596.2:n.1094+269G>A
|
|
ENST00000237596.6:c.1094+269G>A
|
ENSP00000237596.2:n.1094+269G>A
|
|
ENST00000506367.1:n.541+269G>A
|
|
|
NM_000297.3:c.1094+269G>A
|
NP_000288.1:n.1094+269G>A
|
|
XM_011532028.1:c.1094+269G>A
|
XP_011530330.1:n.1094+269G>A
|
|
XM_011532029.1:c.374+269G>A
|
XP_011530331.1:n.374+269G>A
|
|
XM_011532030.1:c.254+269G>A
|
XP_011530332.1:n.254+269G>A
|
|
XR_244632.2:n.1189+269G>A
|
|
|
NR_156488.1:n.1181+269G>A
|
|
|
XM_011532028.2:c.1094+269G>A
|
XP_011530330.1:n.1094+269G>A
|
|
XM_011532030.2:c.254+269G>A
|
XP_011530332.1:n.254+269G>A
|
|
NM_000297.4:c.1094+269G>A
MANE Select
|
NP_000288.1:n.1094+269G>A
|
|
NR_156488.2:n.1193+269G>A
|
|
|