ENST00000342992.11:c.96825G>A
(TTN)
|
ENSP00000343764.6:p.Leu32275=
|
|
ENST00000342175.11:c.77910G>A
(TTN)
|
ENSP00000340554.6:p.Leu25970=
|
|
ENST00000359218.10:c.77709G>A
(TTN)
|
ENSP00000352154.5:p.Leu25903=
|
|
ENST00000342175.10:c.77910G>A
(TTN)
|
ENSP00000340554.6:p.Leu25970=
|
|
ENST00000342992.10:c.96825G>A
(TTN)
|
ENSP00000343764.6:p.Leu32275=
|
|
ENST00000359218.9:c.77709G>A
(TTN)
|
ENSP00000352154.5:p.Leu25903=
|
|
ENST00000460472.6:c.77334G>A
(TTN)
|
ENSP00000434586.1:p.Leu25778=
|
|
ENST00000589042.5:c.104529G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu34843=
|
|
ENST00000591111.5:c.99606G>A
(TTN)
|
ENSP00000465570.1:p.Leu33202=
|
|
ENST00000615779.4:c.99606G>A
(TTN)
|
ENSP00000483597.1:p.Leu33202=
|
|
NM_001256850.1:c.99606G>A
(TTN)
|
NP_001243779.1:p.Leu33202=
|
|
NM_001267550.2:c.104529G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu34843=
|
|
NM_003319.4:c.77334G>A
(TTN)
|
NP_003310.4:p.Leu25778=
|
|
NM_133378.4:c.96825G>A
(TTN)
|
NP_596869.4:p.Leu32275=
|
|
NM_133432.3:c.77709G>A
(TTN)
|
NP_597676.3:p.Leu25903=
|
|
NM_133437.4:c.77910G>A
(TTN)
|
NP_597681.4:p.Leu25970=
|
|
NR_038271.1:n.446+8450C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3646C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103626G>A
(TTN)
|
XP_011510031.1:p.Leu34542=
|
|
XM_011511730.1:c.77520G>A
(TTN)
|
XP_011510032.1:p.Leu25840=
|
|
XM_011511731.1:c.77379G>A
(TTN)
|
XP_011510033.1:p.Leu25793=
|
|
XM_017004819.1:c.103422G>A
(TTN)
|
XP_016860308.1:p.Leu34474=
|
|
XM_017004820.1:c.98820G>A
(TTN)
|
XP_016860309.1:p.Leu32940=
|
|
XM_017004821.1:c.98817G>A
(TTN)
|
XP_016860310.1:p.Leu32939=
|
|
XM_017004822.1:c.95859G>A
(TTN)
|
XP_016860311.1:p.Leu31953=
|
|
XM_017004823.1:c.77475G>A
(TTN)
|
XP_016860312.1:p.Leu25825=
|
|
XM_024453094.1:c.98970G>A
(TTN)
|
XP_024308862.1:p.Leu32990=
|
|
XM_024453095.1:c.98967G>A
(TTN)
|
XP_024308863.1:p.Leu32989=
|
|
XM_024453096.1:c.98400G>A
(TTN)
|
XP_024308864.1:p.Leu32800=
|
|
XM_024453097.1:c.95742G>A
(TTN)
|
XP_024308865.1:p.Leu31914=
|
|
XM_024453098.1:c.95661G>A
(TTN)
|
XP_024308866.1:p.Leu31887=
|
|
XM_024453099.1:c.77424G>A
(TTN)
|
XP_024308867.1:p.Leu25808=
|
|
XM_024453100.1:c.67278G>A
(TTN)
|
XP_024308868.1:p.Leu22426=
|
|