ENST00000397909.7:c.2637-24558G>A
MANE Select
|
ENSP00000381007.2:n.2637-24558G>A
|
|
ENST00000644176.1:c.1137-24558G>A
|
ENSP00000495503.1:n.1137-24558G>A
|
|
ENST00000397909.6:c.2637-24558G>A
|
ENSP00000381007.2:n.2637-24558G>A
|
|
ENST00000536525.6:c.2637-24558G>A
|
ENSP00000446132.2:n.2637-24558G>A
|
|
NM_001024383.1:c.2637-24558G>A
|
NP_001019554.1:n.2637-24558G>A
|
|
NM_014903.5:c.2637-24558G>A
|
NP_055718.4:n.2637-24558G>A
|
|
XM_005269215.2:c.2637-24558G>A
|
XP_005269272.1:n.2637-24558G>A
|
|
XM_006719675.2:c.2568-24558G>A
|
XP_006719738.1:n.2568-24558G>A
|
|
XM_006719677.2:c.1137-24558G>A
|
XP_006719740.1:n.1137-24558G>A
|
|
XM_011538940.1:c.2637-24558G>A
|
XP_011537242.1:n.2637-24558G>A
|
|
XM_011538941.1:c.2637-24558G>A
|
XP_011537243.1:n.2637-24558G>A
|
|
XM_011538942.1:c.2466-24558G>A
|
XP_011537244.1:n.2466-24558G>A
|
|
XM_011538943.1:c.2637-24558G>A
|
XP_011537245.1:n.2637-24558G>A
|
|
XM_011538944.1:c.2637-24558G>A
|
XP_011537246.1:n.2637-24558G>A
|
|
XM_011538945.1:c.1908-24558G>A
|
XP_011537247.1:n.1908-24558G>A
|
|
XM_005269215.4:c.2637-24558G>A
|
XP_005269272.1:n.2637-24558G>A
|
|
XM_011538940.2:c.2637-24558G>A
|
XP_011537242.1:n.2637-24558G>A
|
|
XM_011538941.2:c.2637-24558G>A
|
XP_011537243.1:n.2637-24558G>A
|
|
XM_011538944.3:c.2637-24558G>A
|
XP_011537246.1:n.2637-24558G>A
|
|
XM_017020164.2:c.2637-24558G>A
|
XP_016875653.1:n.2637-24558G>A
|
|
XM_017020165.1:c.2637-24558G>A
|
XP_016875654.1:n.2637-24558G>A
|
|
XM_017020166.2:c.2466-24558G>A
|
XP_016875655.1:n.2466-24558G>A
|
|
XM_017020167.1:c.2397-24558G>A
|
XP_016875656.1:n.2397-24558G>A
|
|
XM_017020168.1:c.2637-24558G>A
|
XP_016875657.1:n.2637-24558G>A
|
|
XM_017020169.2:c.2637-24558G>A
|
XP_016875658.1:n.2637-24558G>A
|
|
XM_017020170.1:c.2637-24558G>A
|
XP_016875659.1:n.2637-24558G>A
|
|
XM_017020171.1:c.1137-24558G>A
|
XP_016875660.1:n.1137-24558G>A
|
|
XM_017020172.1:c.1137-24558G>A
|
XP_016875661.1:n.1137-24558G>A
|
|
XM_017020173.2:c.1137-24558G>A
|
XP_016875662.1:n.1137-24558G>A
|
|
XM_017020174.1:c.1137-24558G>A
|
XP_016875663.1:n.1137-24558G>A
|
|
XM_017020175.1:c.1137-24558G>A
|
XP_016875664.1:n.1137-24558G>A
|
|
NM_001024383.2:c.2637-24558G>A
MANE Select
|
NP_001019554.1:n.2637-24558G>A
|
|
NM_014903.6:c.2637-24558G>A
|
NP_055718.4:n.2637-24558G>A
|
|