ENST00000375754.9:c.1836-2759G>A
MANE Select
|
ENSP00000364907.4:n.1836-2759G>A
|
|
ENST00000375746.1:c.1836-2759G>A
|
ENSP00000364898.1:n.1836-2759G>A
|
|
ENST00000375747.5:c.1767-2759G>A
|
ENSP00000364899.1:n.1767-2759G>A
|
|
ENST00000375751.8:c.1767-2759G>A
|
ENSP00000364904.4:n.1767-2759G>A
|
|
ENST00000375754.8:c.1836-2759G>A
|
ENSP00000364907.4:n.1836-2759G>A
|
|
NM_001135052.3:c.1767-2759G>A
|
NP_001128524.1:n.1767-2759G>A
|
|
NM_001174167.2:c.1836-2759G>A
|
NP_001167638.1:n.1836-2759G>A
|
|
NM_001174168.2:c.1767-2759G>A
|
NP_001167639.1:n.1767-2759G>A
|
|
NM_003177.6:c.1836-2759G>A
|
NP_003168.2:n.1836-2759G>A
|
|
XM_005252147.2:c.1836-2759G>A
|
XP_005252204.1:n.1836-2759G>A
|
|
XM_011518946.1:c.1836-2759G>A
|
XP_011517248.1:n.1836-2759G>A
|
|
XM_011518947.1:c.1767-2759G>A
|
XP_011517249.1:n.1767-2759G>A
|
|
XM_005252147.4:c.1836-2759G>A
|
XP_005252204.1:n.1836-2759G>A
|
|
XM_011518946.3:c.1836-2759G>A
|
XP_011517248.1:n.1836-2759G>A
|
|
XR_001746370.2:n.2039-2759G>A
|
|
|
NM_003177.7:c.1836-2759G>A
MANE Select
|
NP_003168.2:n.1836-2759G>A
|
|
NM_001135052.4:c.1767-2759G>A
|
NP_001128524.1:n.1767-2759G>A
|
|
NM_001174167.3:c.1836-2759G>A
|
NP_001167638.1:n.1836-2759G>A
|
|
NM_001174168.3:c.1767-2759G>A
|
NP_001167639.1:n.1767-2759G>A
|
|