ENST00000403665.7:c.1685del
(F11)
MANE Select
|
ENSP00000384957.2:p.Gly562AlafsTer29
|
|
ENST00000264691.4:c.285del
(F11)
|
|
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ENST00000264692.8:c.1523del
(F11)
|
ENSP00000264692.5:p.Gly508AlafsTer29
|
|
ENST00000403665.6:c.1685del
(F11)
|
ENSP00000384957.2:p.Gly562AlafsTer29
|
|
ENST00000503841.1:n.204del
(F11)
|
|
|
NM_000128.3:c.1685del , LRG_583t1:c.1685del
(F11)
|
NP_000119.1:p.Gly562AlafsTer29
|
|
NR_033900.1:n.1066+637del
(F11-AS1)
|
|
|
XM_005262821.2:c.1688del
(F11)
|
XP_005262878.1:p.Gly563AlafsTer29
|
|
XM_005262822.2:c.1592del
(F11)
|
XP_005262879.1:p.Gly531AlafsTer29
|
|
XM_005262823.2:c.1418del
(F11)
|
XP_005262880.1:p.Gly473AlafsTer29
|
|
XM_006714137.1:c.1640del
(F11)
|
XP_006714200.1:p.Gly547AlafsTer29
|
|
XM_005262821.4:c.1688del
(F11)
|
XP_005262878.1:p.Gly563AlafsTer29
|
|
XM_005262822.4:c.1592del
(F11)
|
XP_005262879.1:p.Gly531AlafsTer29
|
|
XM_005262823.4:c.1418del
(F11)
|
XP_005262880.1:p.Gly473AlafsTer29
|
|
XM_006714137.3:c.1640del
(F11)
|
XP_006714200.1:p.Gly547AlafsTer29
|
|
NM_000128.4:c.1685del
(F11)
MANE Select
|
NP_000119.1:p.Gly562AlafsTer29
|
|