ENST00000350721.9:c.6319+106G>T
MANE Select
|
ENSP00000343741.4:n.6319+106G>T
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|
ENST00000513291.2:n.1503+106G>T
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|
|
ENST00000654170.1:n.1162+106G>T
|
|
|
ENST00000656590.1:c.5109+106G>T
|
|
|
ENST00000661310.1:c.6127+106G>T
|
ENSP00000499589.1:n.6127+106G>T
|
|
ENST00000665483.1:n.174+106G>T
|
|
|
ENST00000666447.1:n.154+106G>T
|
|
|
ENST00000666943.1:n.1783+106G>T
|
|
|
ENST00000350721.8:c.6319+106G>T
|
ENSP00000343741.4:n.6319+106G>T
|
|
NM_001184.3:c.6319+106G>T
|
NP_001175.2:n.6319+106G>T
|
|
XM_011512924.1:c.6325+106G>T
|
XP_011511226.1:n.6325+106G>T
|
|
XM_011512925.1:c.6133+106G>T
|
XP_011511227.1:n.6133+106G>T
|
|
XR_924147.1:n.6414+106G>T
|
|
|
XR_924148.1:n.6414+106G>T
|
|
|
XR_924149.1:n.6293+106G>T
|
|
|
NM_001354579.1:c.6127+106G>T
|
NP_001341508.1:n.6127+106G>T
|
|
XR_001740179.2:n.6408+106G>T
|
|
|
XR_001740180.2:n.6462+106G>T
|
|
|
XR_001740181.2:n.6341+106G>T
|
|
|
XR_001740182.1:n.6293+106G>T
|
|
|
XR_002959543.1:n.6518+106G>T
|
|
|
XR_924148.2:n.6414+106G>T
|
|
|
NM_001184.4:c.6319+106G>T
MANE Select
|
NP_001175.2:n.6319+106G>T
|
|
NM_001354579.2:c.6127+106G>T
|
NP_001341508.1:n.6127+106G>T
|
|