ENST00000648319.1:c.160-774A>C
MANE Select
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ENSP00000496939.1:n.160-774A>C
|
|
ENST00000262888.7:c.160-774A>C
|
ENSP00000262888.3:n.160-774A>C
|
|
ENST00000599720.5:c.159+3293A>C
|
ENSP00000472513.1:n.159+3293A>C
|
|
ENST00000615047.4:c.-26-774A>C
|
ENSP00000485014.1:n.-26-774A>C
|
|
NM_002250.2:c.160-774A>C
|
NP_002241.1:n.160-774A>C
|
|
XM_005258882.2:c.160-2791A>C
|
XP_005258939.1:n.160-2791A>C
|
|
XM_005258883.2:c.-26-774A>C
|
XP_005258940.1:n.-26-774A>C
|
|
XM_011526938.1:c.160-774A>C
|
XP_011525240.1:n.160-774A>C
|
|
XR_935823.1:n.1438-774A>C
|
|
|
XR_002958313.1:n.1438-774A>C
|
|
|
NM_002250.3:c.160-774A>C
MANE Select
|
NP_002241.1:n.160-774A>C
|
|