ENST00000361383.11:c.1312-1047G>T
MANE Select
|
ENSP00000355050.6:n.1312-1047G>T
|
|
ENST00000361383.10:c.1312-1047G>T
|
ENSP00000355050.6:n.1312-1047G>T
|
|
ENST00000373469.1:c.556-1047G>T
|
ENSP00000362568.1:n.556-1047G>T
|
|
ENST00000373473.5:c.751-1047G>T
|
ENSP00000362572.1:n.751-1047G>T
|
|
ENST00000405275.6:c.1231-1047G>T
|
ENSP00000384355.2:n.1231-1047G>T
|
|
ENST00000473857.5:n.2494-1047G>T
|
|
|
ENST00000621317.4:c.1327-1047G>T
|
ENSP00000478532.1:n.1327-1047G>T
|
|
ENST00000628103.2:c.1231-1047G>T
|
ENSP00000487198.1:n.1231-1047G>T
|
|
NM_001281495.1:c.1231-1047G>T
|
NP_001268424.1:n.1231-1047G>T
|
|
NM_030877.4:c.1312-1047G>T
|
NP_110517.2:n.1312-1047G>T
|
|
XM_011528917.1:c.982-1047G>T
|
XP_011527219.1:n.982-1047G>T
|
|
XM_011528917.2:c.982-1047G>T
|
XP_011527219.1:n.982-1047G>T
|
|
XM_024451947.1:c.1231-1047G>T
|
XP_024307715.1:n.1231-1047G>T
|
|
NM_030877.5:c.1312-1047G>T
MANE Select
|
NP_110517.2:n.1312-1047G>T
|
|
NM_001281495.2:c.1231-1047G>T
|
NP_001268424.1:n.1231-1047G>T
|
|