ENST00000651487.1:c.-23+2391G>T
MANE Select
|
ENSP00000498976.1:n.-23+2391G>T
|
|
ENST00000332427.6:c.-23+2391G>T
|
ENSP00000333744.2:n.-23+2391G>T
|
|
ENST00000540510.1:c.-23+2391G>T
|
ENSP00000441832.1:n.-23+2391G>T
|
|
ENST00000540796.5:c.-23+2391G>T
|
ENSP00000441963.1:n.-23+2391G>T
|
|
NM_006143.2:c.-23+2391G>T
|
NP_006134.1:n.-23+2391G>T
|
|
XM_011520622.1:c.6+2391G>T
|
XP_011518924.1:n.6+2391G>T
|
|
XM_011520623.1:c.6+2391G>T
|
XP_011518925.1:n.6+2391G>T
|
|
XM_011520624.1:c.6+2391G>T
|
XP_011518926.1:n.6+2391G>T
|
|
XM_011520625.1:c.-162+2391G>T
|
XP_011518927.1:n.-162+2391G>T
|
|
XM_011520626.1:c.562+2391G>T
|
XP_011518928.1:n.562+2391G>T
|
|
XM_011520623.3:c.6+2391G>T
|
XP_011518925.1:n.6+2391G>T
|
|
XM_011520624.2:c.6+2391G>T
|
XP_011518926.1:n.6+2391G>T
|
|
XM_011520625.2:c.-162+2391G>T
|
XP_011518927.1:n.-162+2391G>T
|
|
XM_017019212.1:c.6+2391G>T
|
XP_016874701.1:n.6+2391G>T
|
|
XM_017019213.1:c.6+2391G>T
|
XP_016874702.1:n.6+2391G>T
|
|
XM_017019214.1:c.6+2391G>T
|
XP_016874703.1:n.6+2391G>T
|
|
XM_017019216.2:c.-23+2391G>T
|
XP_016874705.1:n.-23+2391G>T
|
|
NM_006143.3:c.-23+2391G>T
MANE Select
|
NP_006134.2:n.-23+2391G>T
|
|