NM_024120.5:c.-26G>T
MANE Select
|
NP_077025.2:n.-26G>T
|
ENST00000378106.10:c.-26G>T
MANE Select
|
ENSP00000367346.5:n.-26G>T
|
NM_001039375.2:c.-26G>T
|
NP_001034464.1:n.-26G>T
|
NM_001039375.3:c.-26G>T
|
NP_001034464.1:n.-26G>T
|
NM_001352403.1:c.-393G>T
|
NP_001339332.1:n.-393G>T
|
NM_001352403.2:c.-393G>T
|
NP_001339332.1:n.-393G>T
|
NM_001352406.1:c.-607G>T
|
NP_001339335.1:n.-607G>T
|
NM_001352406.2:c.-607G>T
|
NP_001339335.1:n.-607G>T
|
NM_001352407.1:c.-721G>T
|
NP_001339336.1:n.-721G>T
|
NM_001352407.2:c.-721G>T
|
NP_001339336.1:n.-721G>T
|
NM_001352408.1:c.-26G>T
|
NP_001339337.1:n.-26G>T
|
NM_001352408.2:c.-26G>T
|
NP_001339337.1:n.-26G>T
|
NM_024120.4:c.-26G>T
|
NP_077025.2:n.-26G>T
|
NR_029377.1:n.18G>T
|
|
NR_029377.2:n.16G>T
|
|
NR_147978.1:n.18G>T
|
|
NR_147978.2:n.16G>T
|
|
NR_147979.1:n.18G>T
|
|
NR_147979.2:n.16G>T
|
|
NR_147980.1:n.18G>T
|
|
NR_147980.2:n.16G>T
|
|
NR_147981.1:n.18G>T
|
|
NR_147981.2:n.16G>T
|
|
NR_147982.1:n.18G>T
|
|
NR_147982.2:n.16G>T
|
|
NR_147983.1:n.18G>T
|
|
NR_147983.2:n.16G>T
|
|
ENST00000378081.9:c.-26G>T
|
ENSP00000437325.1:n.-26G>T
|
ENST00000378106.9:c.-26G>T
|
ENSP00000367346.5:n.-26G>T
|
XM_006723622.2:c.-393G>T
|
XP_006723685.1:n.-393G>T
|
XM_006723624.1:c.-527G>T
|
XP_006723687.1:n.-527G>T
|
XM_006723624.2:c.-527G>T
|
XP_006723687.1:n.-527G>T
|
XR_001754396.1:n.18G>T
|
|