ENST00000308182.10:c.4737+19dup
MANE Select
|
ENSP00000310435.6:n.4737+19dup
|
|
ENST00000475866.3:c.5709+19dup
|
ENSP00000428746.2:n.5709+19dup
|
|
ENST00000308182.9:c.4737+19dup
|
ENSP00000310435.6:n.4737+19dup
|
|
ENST00000374208.1:n.215+19dup
|
|
|
ENST00000374211.5:n.351+19dup
|
|
|
ENST00000527815.5:c.2115+19dup
|
ENSP00000433931.1:n.2115+19dup
|
|
NM_001039775.3:c.4737+19dup
|
NP_001034864.2:n.4737+19dup
|
|
XM_005245918.2:c.4737+19dup
|
XP_005245975.1:n.4737+19dup
|
|
XM_011541672.1:c.4701+19dup
|
XP_011539974.1:n.4701+19dup
|
|
XM_011541673.1:c.4908+19dup
|
XP_011539975.1:n.4908+19dup
|
|
XR_946681.1:n.5201+19dup
|
|
|
XM_011541673.2:c.4908+19dup
|
XP_011539975.1:n.4908+19dup
|
|
XR_001737260.1:n.4760+19dup
|
|
|
NM_001039775.4:c.4737+19dup
MANE Select
|
NP_001034864.2:n.4737+19dup
|
|