|
ENST00000403665.7:c.1823_1824insATTTA
(F11)
MANE Select
|
ENSP00000384957.2:p.Tyr608Ter
|
|
|
ENST00000264691.4:c.423_424insATTTA
(F11)
|
|
|
|
ENST00000264692.8:c.1661_1662insATTTA
(F11)
|
ENSP00000264692.5:p.Tyr554Ter
|
|
|
ENST00000403665.6:c.1823_1824insATTTA
(F11)
|
ENSP00000384957.2:p.Tyr608Ter
|
|
|
ENST00000503841.1:n.342_343insATTTA
(F11)
|
|
|
|
NM_000128.3:c.1823_1824insATTTA , LRG_583t1:c.1823_1824insATTTA
(F11)
|
NP_000119.1:p.Tyr608Ter
|
|
|
NR_033900.1:n.938_939insTTAAA
(F11-AS1)
|
|
|
|
XM_005262821.2:c.1826_1827insATTTA
(F11)
|
XP_005262878.1:p.Tyr609Ter
|
|
|
XM_005262822.2:c.1730_1731insATTTA
(F11)
|
XP_005262879.1:p.Tyr577Ter
|
|
|
XM_005262823.2:c.1556_1557insATTTA
(F11)
|
XP_005262880.1:p.Tyr519Ter
|
|
|
XM_006714137.1:c.1778_1779insATTTA
(F11)
|
XP_006714200.1:p.Tyr593Ter
|
|
|
XM_005262821.4:c.1826_1827insATTTA
(F11)
|
XP_005262878.1:p.Tyr609Ter
|
|
|
XM_005262822.4:c.1730_1731insATTTA
(F11)
|
XP_005262879.1:p.Tyr577Ter
|
|
|
XM_005262823.4:c.1556_1557insATTTA
(F11)
|
XP_005262880.1:p.Tyr519Ter
|
|
|
XM_006714137.3:c.1778_1779insATTTA
(F11)
|
XP_006714200.1:p.Tyr593Ter
|
|
|
NM_000128.4:c.1823_1824insATTTA
(F11)
MANE Select
|
NP_000119.1:p.Tyr608Ter
|
|
