ENST00000237596.7:c.844-38G>T
MANE Select
|
ENSP00000237596.2:n.844-38G>T
|
|
ENST00000237596.6:c.844-38G>T
|
ENSP00000237596.2:n.844-38G>T
|
|
ENST00000506367.1:n.291-38G>T
|
|
|
ENST00000506727.1:n.430-38G>T
|
|
|
NM_000297.3:c.844-38G>T
|
NP_000288.1:n.844-38G>T
|
|
XM_011532028.1:c.844-38G>T
|
XP_011530330.1:n.844-38G>T
|
|
XM_011532029.1:c.124-38G>T
|
XP_011530331.1:n.124-38G>T
|
|
XM_011532030.1:c.4-38G>T
|
XP_011530332.1:n.4-38G>T
|
|
XR_244632.2:n.939-38G>T
|
|
|
NR_156488.1:n.931-38G>T
|
|
|
XM_011532028.2:c.844-38G>T
|
XP_011530330.1:n.844-38G>T
|
|
XM_011532030.2:c.4-38G>T
|
XP_011530332.1:n.4-38G>T
|
|
NM_000297.4:c.844-38G>T
MANE Select
|
NP_000288.1:n.844-38G>T
|
|
NR_156488.2:n.943-38G>T
|
|
|