ENST00000355808.10:c.*497G>A
(PDHA1)
|
ENSP00000348062.6:n.*497G>A
|
|
ENST00000423505.6:c.*497G>A
(PDHA1)
|
ENSP00000406473.2:n.*497G>A
|
|
ENST00000696704.1:c.*1002G>A
(PDHA1)
|
ENSP00000512823.1:n.*1002G>A
|
|
ENST00000696705.1:c.*1125G>A
(PDHA1)
|
ENSP00000512824.1:n.*1125G>A
|
|
ENST00000338883.9:c.*599C>T
(MAP3K15)
MANE Select
|
ENSP00000345629.4:n.*599C>T
|
|
ENST00000422285.7:c.*497G>A
(PDHA1)
MANE Select
|
ENSP00000394382.2:n.*497G>A
|
|
ENST00000359173.7:c.3869C>T
(MAP3K15)
|
|
|
ENST00000379806.9:c.*497G>A
(PDHA1)
|
ENSP00000369134.5:n.*497G>A
|
|
ENST00000422285.6:c.*497G>A
(PDHA1)
|
ENSP00000394382.2:n.*497G>A
|
|
ENST00000470101.1:n.1959C>T
(MAP3K15)
|
|
|
ENST00000518578.5:n.4603C>T
(MAP3K15)
|
|
|
ENST00000540249.5:c.*497G>A
(PDHA1)
|
ENSP00000440761.1:n.*497G>A
|
|
ENST00000545074.5:c.*497G>A
(PDHA1)
|
ENSP00000438550.1:n.*497G>A
|
|
NM_000284.3:c.*497G>A
(PDHA1)
|
NP_000275.1:n.*497G>A
|
|
NM_001001671.3:c.4541C>T
(MAP3K15)
|
NP_001001671.3:n.4541C>T
|
|
NM_001173454.1:c.*497G>A
(PDHA1)
|
NP_001166925.1:n.*497G>A
|
|
NM_001173455.1:c.*497G>A
(PDHA1)
|
NP_001166926.1:n.*497G>A
|
|
NM_001173456.1:c.*497G>A
(PDHA1)
|
NP_001166927.1:n.*497G>A
|
|
XM_011545507.1:c.*599C>T
(MAP3K15)
|
XP_011543809.1:n.*599C>T
|
|
XM_011545508.1:c.*599C>T
(MAP3K15)
|
XP_011543810.1:n.*599C>T
|
|
XM_011545509.1:c.*599C>T
(MAP3K15)
|
XP_011543811.1:n.*599C>T
|
|
XM_011545510.1:c.*599C>T
(MAP3K15)
|
XP_011543812.1:n.*599C>T
|
|
XM_011545511.1:c.*599C>T
(MAP3K15)
|
XP_011543813.1:n.*599C>T
|
|
XM_011545531.1:c.*497G>A
(PDHA1)
|
XP_011543833.1:n.*497G>A
|
|
XM_011545532.1:c.*497G>A
(PDHA1)
|
XP_011543834.1:n.*497G>A
|
|
XM_011545507.3:c.*599C>T
(MAP3K15)
|
XP_011543809.3:n.*599C>T
|
|
XM_011545508.3:c.*599C>T
(MAP3K15)
|
XP_011543810.3:n.*599C>T
|
|
XM_011545510.2:c.*599C>T
(MAP3K15)
|
XP_011543812.1:n.*599C>T
|
|
XM_011545511.2:c.*599C>T
(MAP3K15)
|
XP_011543813.1:n.*599C>T
|
|
NM_000284.4:c.*497G>A
(PDHA1)
MANE Select
|
NP_000275.1:n.*497G>A
|
|
NM_001001671.4:c.*599C>T
(MAP3K15)
MANE Select
|
NP_001001671.3:n.*599C>T
|
|
NM_001173454.2:c.*497G>A
(PDHA1)
|
NP_001166925.1:n.*497G>A
|
|
NM_001173455.2:c.*497G>A
(PDHA1)
|
NP_001166926.1:n.*497G>A
|
|
NM_001173456.2:c.*497G>A
(PDHA1)
|
NP_001166927.1:n.*497G>A
|
|