ENST00000350721.9:c.6319+5A>G
MANE Select
|
ENSP00000343741.4:n.6319+5A>G
|
|
ENST00000513291.2:n.1503+5A>G
|
|
|
ENST00000654170.1:n.1162+5A>G
|
|
|
ENST00000656590.1:c.5109+5A>G
|
|
|
ENST00000661310.1:c.6127+5A>G
|
ENSP00000499589.1:n.6127+5A>G
|
|
ENST00000665483.1:n.174+5A>G
|
|
|
ENST00000666447.1:n.154+5A>G
|
|
|
ENST00000666943.1:n.1783+5A>G
|
|
|
ENST00000350721.8:c.6319+5A>G
|
ENSP00000343741.4:n.6319+5A>G
|
|
NM_001184.3:c.6319+5A>G
|
NP_001175.2:n.6319+5A>G
|
|
XM_011512924.1:c.6325+5A>G
|
XP_011511226.1:n.6325+5A>G
|
|
XM_011512925.1:c.6133+5A>G
|
XP_011511227.1:n.6133+5A>G
|
|
XR_924147.1:n.6414+5A>G
|
|
|
XR_924148.1:n.6414+5A>G
|
|
|
XR_924149.1:n.6293+5A>G
|
|
|
NM_001354579.1:c.6127+5A>G
|
NP_001341508.1:n.6127+5A>G
|
|
XR_001740179.2:n.6408+5A>G
|
|
|
XR_001740180.2:n.6462+5A>G
|
|
|
XR_001740181.2:n.6341+5A>G
|
|
|
XR_001740182.1:n.6293+5A>G
|
|
|
XR_002959543.1:n.6518+5A>G
|
|
|
XR_924148.2:n.6414+5A>G
|
|
|
NM_001184.4:c.6319+5A>G
MANE Select
|
NP_001175.2:n.6319+5A>G
|
|
NM_001354579.2:c.6127+5A>G
|
NP_001341508.1:n.6127+5A>G
|
|