ENST00000399286.3:c.-161-10678G>C
MANE Select
|
ENSP00000382226.2:n.-161-10678G>C
|
|
ENST00000337385.7:c.-161-10678G>C
|
ENSP00000337255.3:n.-161-10678G>C
|
|
ENST00000399284.1:c.-133-10706G>C
|
ENSP00000382225.1:n.-133-10706G>C
|
|
ENST00000399286.2:c.-161-10678G>C
|
ENSP00000382226.2:n.-161-10678G>C
|
|
ENST00000611936.1:c.-50-19758G>C
|
ENSP00000478215.1:n.-50-19758G>C
|
|
NM_000219.5:c.-161-10678G>C
|
NP_000210.2:n.-161-10678G>C
|
|
NM_001270402.2:c.-161-10678G>C
|
NP_001257331.1:n.-161-10678G>C
|
|
NM_001270403.2:c.-133-10706G>C
|
NP_001257332.1:n.-133-10706G>C
|
|
NM_001270404.2:c.-50-19758G>C
|
NP_001257333.1:n.-50-19758G>C
|
|
XM_011529557.1:c.169-10678G>C
|
XP_011527859.1:n.169-10678G>C
|
|
NM_000219.6:c.-161-10678G>C
MANE Select
|
NP_000210.2:n.-161-10678G>C
|
|
NM_001270402.3:c.-161-10678G>C
|
NP_001257331.1:n.-161-10678G>C
|
|
NM_001270404.3:c.-50-19758G>C
|
NP_001257333.1:n.-50-19758G>C
|
|