ENST00000696526.1:c.3123G>T
MANE Select
|
ENSP00000512689.1:p.Leu1041Phe
|
|
ENST00000644968.1:c.3123G>T
|
ENSP00000496254.1:p.Leu1041Phe
|
|
ENST00000358517.6:c.3123G>T
|
ENSP00000351318.2:p.Leu1041Phe
|
|
ENST00000367328.5:c.3123G>T
|
ENSP00000356297.1:p.Leu1041Phe
|
|
ENST00000475490.1:c.1158-1174G>T
|
ENSP00000433107.1:n.1158-1174G>T
|
|
NM_001029884.1:c.3123G>T
|
NP_001025055.1:p.Leu1041Phe
|
|
XM_005267064.2:c.3300G>T
|
XP_005267121.1:p.Leu1100Phe
|
|
XM_005267065.2:c.3123G>T
|
XP_005267122.1:p.Leu1041Phe
|
|
XM_005267066.1:c.3123G>T
|
XP_005267123.1:p.Leu1041Phe
|
|
XM_006715521.1:c.3123G>T
|
XP_006715584.1:p.Leu1041Phe
|
|
XM_006715522.2:c.3123G>T
|
XP_006715585.1:p.Leu1041Phe
|
|
XM_011535981.1:c.3339G>T
|
XP_011534283.1:p.Leu1113Phe
|
|
XM_011535982.1:c.3300G>T
|
XP_011534284.1:p.Leu1100Phe
|
|
XM_011535983.1:c.3123G>T
|
XP_011534285.1:p.Leu1041Phe
|
|
NM_001029884.2:c.3123G>T
|
NP_001025055.1:p.Leu1041Phe
|
|
NM_001329798.1:c.3300G>T
|
NP_001316727.1:p.Leu1100Phe
|
|
NM_001329799.1:c.3243G>T
|
NP_001316728.1:p.Leu1081Phe
|
|
NM_001329800.1:c.3123G>T
|
NP_001316729.1:p.Leu1041Phe
|
|
NM_001329801.1:c.3123G>T
|
NP_001316730.1:p.Leu1041Phe
|
|
NM_001329802.1:c.3084G>T
|
NP_001316731.1:p.Leu1028Phe
|
|
NM_001329803.1:c.3006G>T
|
NP_001316732.1:p.Leu1002Phe
|
|
NM_001329804.1:c.1617-1174G>T
|
NP_001316733.1:n.1617-1174G>T
|
|
NM_001329805.1:c.1617-1174G>T
|
NP_001316734.1:n.1617-1174G>T
|
|
NM_001329806.1:c.1617-1174G>T
|
NP_001316735.1:n.1617-1174G>T
|
|
NM_001029884.3:c.3123G>T
MANE Select
|
NP_001025055.1:p.Leu1041Phe
|
|
NM_001329798.2:c.3300G>T
|
NP_001316727.1:p.Leu1100Phe
|
|
NM_001329799.2:c.3243G>T
|
NP_001316728.1:p.Leu1081Phe
|
|
NM_001329800.2:c.3123G>T
|
NP_001316729.1:p.Leu1041Phe
|
|
NM_001329801.2:c.3123G>T
|
NP_001316730.1:p.Leu1041Phe
|
|
NM_001329802.2:c.3084G>T
|
NP_001316731.1:p.Leu1028Phe
|
|
NM_001329803.2:c.3006G>T
|
NP_001316732.1:p.Leu1002Phe
|
|
NM_001329804.2:c.1617-1174G>T
|
NP_001316733.1:n.1617-1174G>T
|
|
NM_001329805.2:c.1617-1174G>T
|
NP_001316734.1:n.1617-1174G>T
|
|
NM_001329806.2:c.1617-1174G>T
|
NP_001316735.1:n.1617-1174G>T
|
|