|
ENST00000260649.11:c.1843C>A
(SLC3A1)
MANE Select
|
ENSP00000260649.6:p.Pro615Thr
|
|
|
ENST00000409411.6:c.*932G>T
(PREPL)
MANE Select
|
ENSP00000387095.2:n.*932G>T
|
|
|
ENST00000260649.10:c.1843C>A
(SLC3A1)
|
ENSP00000260649.6:p.Pro615Thr
|
|
|
ENST00000409380.5:c.1009C>A
(SLC3A1)
|
ENSP00000386709.1:p.Pro337Thr
|
|
|
ENST00000409411.5:c.*932G>T
(PREPL)
|
ENSP00000387095.1:n.*932G>T
|
|
|
ENST00000409740.3:c.736C>A
(SLC3A1)
|
ENSP00000386677.3:p.Pro246Thr
|
|
|
ENST00000409936.5:c.*932G>T
(PREPL)
|
ENSP00000386543.1:n.*932G>T
|
|
|
ENST00000409957.5:c.*932G>T
(PREPL)
|
ENSP00000387241.1:n.*932G>T
|
|
|
ENST00000425263.5:c.*932G>T
(PREPL)
|
ENSP00000391456.1:n.*932G>T
|
|
|
ENST00000426481.5:c.*932G>T
(PREPL)
|
ENSP00000409480.1:n.*932G>T
|
|
|
ENST00000444696.5:c.425G>T
(PREPL)
|
ENSP00000390618.1:n.425G>T
|
|
|
ENST00000541738.5:c.*932G>T
(PREPL)
|
ENSP00000439626.1:n.*932G>T
|
|
|
NM_000341.3:c.1843C>A
(SLC3A1)
|
NP_000332.2:p.Pro615Thr
|
|
|
NM_001042385.2:c.*932G>T
(PREPL)
|
NP_001035844.1:n.*932G>T
|
|
|
NM_001042386.2:c.*932G>T
(PREPL)
|
NP_001035845.1:n.*932G>T
|
|
|
NM_001171603.1:c.*932G>T
(PREPL)
|
NP_001165074.1:n.*932G>T
|
|
|
NM_001171606.1:c.*932G>T
(PREPL)
|
NP_001165077.1:n.*932G>T
|
|
|
NM_001171613.1:c.*932G>T
(PREPL)
|
NP_001165084.1:n.*932G>T
|
|
|
NM_001171617.1:c.*932G>T
(PREPL)
|
NP_001165088.1:n.*932G>T
|
|
|
NM_006036.4:c.*932G>T
(PREPL)
|
NP_006027.2:n.*932G>T
|
|
|
XM_011533198.1:c.*932G>T
(PREPL)
|
XP_011531500.1:n.*932G>T
|
|
|
XM_011533199.1:c.*932G>T
(PREPL)
|
XP_011531501.1:n.*932G>T
|
|
|
XM_011533200.1:c.*932G>T
(PREPL)
|
XP_011531502.1:n.*932G>T
|
|
|
XM_011533201.1:c.*1005G>T
(PREPL)
|
XP_011531503.1:n.*1005G>T
|
|
|
XM_011533202.1:c.*932G>T
(PREPL)
|
XP_011531504.1:n.*932G>T
|
|
|
XM_011533047.3:c.*2229C>A
(SLC3A1)
|
XP_011531349.1:n.*2229C>A
|
|
|
XM_011533198.2:c.*932G>T
(PREPL)
|
XP_011531500.1:n.*932G>T
|
|
|
XM_017005384.1:c.*932G>T
(PREPL)
|
XP_016860873.1:n.*932G>T
|
|
|
XM_017005385.1:c.*932G>T
(PREPL)
|
XP_016860874.1:n.*932G>T
|
|
|
NM_000341.4:c.1843C>A
(SLC3A1)
MANE Select
|
NP_000332.2:p.Pro615Thr
|
|
|
NM_001171613.2:c.*932G>T
(PREPL)
MANE Select
|
NP_001165084.1:n.*932G>T
|
|
|
NM_001374275.1:c.*932G>T
(PREPL)
|
NP_001361204.1:n.*932G>T
|
|
|
NM_001374276.1:c.*932G>T
(PREPL)
|
NP_001361205.1:n.*932G>T
|
|
|
NM_001374277.1:c.*932G>T
(PREPL)
|
NP_001361206.1:n.*932G>T
|
|
|
NM_001171606.2:c.*932G>T
(PREPL)
|
NP_001165077.1:n.*932G>T
|
|
