ENST00000328963.10:c.-28G>T
MANE Select
|
ENSP00000330696.6:n.-28G>T
|
|
ENST00000261826.10:c.-28G>T
|
ENSP00000261826.6:n.-28G>T
|
|
ENST00000328963.9:c.-28G>T
|
ENSP00000330696.6:n.-28G>T
|
|
ENST00000535928.5:c.-28G>T
|
ENSP00000439961.1:n.-28G>T
|
|
ENST00000537312.5:c.-28G>T
|
ENSP00000438586.1:n.-28G>T
|
|
ENST00000539695.5:n.42G>T
|
|
|
ENST00000545434.5:c.-28G>T
|
ENSP00000445564.1:n.-28G>T
|
|
NM_002562.5:c.-28G>T
|
NP_002553.3:n.-28G>T
|
|
NR_033948.1:n.116G>T
|
|
|
NR_033949.1:n.116G>T
|
|
|
NR_033950.1:n.116G>T
|
|
|
NR_033951.1:n.116G>T
|
|
|
NR_033952.1:n.116G>T
|
|
|
NR_033953.1:n.125G>T
|
|
|
NR_033954.1:n.116G>T
|
|
|
NR_033955.1:n.116G>T
|
|
|
NR_033956.1:n.116G>T
|
|
|
XM_011538418.1:c.-28G>T
|
XP_011536720.1:n.-28G>T
|
|
XM_011538419.1:c.-171G>T
|
XP_011536721.1:n.-171G>T
|
|
XM_011538419.3:c.-171G>T
|
XP_011536721.1:n.-171G>T
|
|
XM_017019364.2:c.-541G>T
|
XP_016874853.1:n.-541G>T
|
|
XM_017019365.2:c.-372G>T
|
XP_016874854.1:n.-372G>T
|
|
XM_017019366.2:c.-708G>T
|
XP_016874855.1:n.-708G>T
|
|
XM_017019367.2:c.-539G>T
|
XP_016874856.1:n.-539G>T
|
|
XR_001749352.2:n.187-6102C>A
|
|
|
XR_001749354.2:n.187-6102C>A
|
|
|
NM_002562.6:c.-28G>T
MANE Select
|
NP_002553.3:n.-28G>T
|
|
NR_033948.2:n.68G>T
|
|
|
NR_033949.2:n.68G>T
|
|
|
NR_033950.2:n.68G>T
|
|
|
NR_033951.2:n.68G>T
|
|
|
NR_033952.2:n.68G>T
|
|
|
NR_033953.2:n.68G>T
|
|
|
NR_033954.2:n.68G>T
|
|
|
NR_033955.2:n.68G>T
|
|
|
NR_033956.2:n.68G>T
|
|
|