ENST00000342992.11:c.60826C>T
(TTN)
|
ENSP00000343764.6:p.Pro20276Ser
|
|
ENST00000342175.11:c.41911C>T
(TTN)
|
ENSP00000340554.6:p.Pro13971Ser
|
|
ENST00000359218.10:c.41710C>T
(TTN)
|
ENSP00000352154.5:p.Pro13904Ser
|
|
ENST00000342175.10:c.41911C>T
(TTN)
|
ENSP00000340554.6:p.Pro13971Ser
|
|
ENST00000342992.10:c.60826C>T
(TTN)
|
ENSP00000343764.6:p.Pro20276Ser
|
|
ENST00000359218.9:c.41710C>T
(TTN)
|
ENSP00000352154.5:p.Pro13904Ser
|
|
ENST00000460472.6:c.41335C>T
(TTN)
|
ENSP00000434586.1:p.Pro13779Ser
|
|
ENST00000589042.5:c.68530C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro22844Ser
|
|
ENST00000591111.5:c.63607C>T
(TTN)
|
ENSP00000465570.1:p.Pro21203Ser
|
|
ENST00000615779.4:c.63607C>T
(TTN)
|
ENSP00000483597.1:p.Pro21203Ser
|
|
NM_001256850.1:c.63607C>T
(TTN)
|
NP_001243779.1:p.Pro21203Ser
|
|
NM_001267550.2:c.68530C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Pro22844Ser
|
|
NM_003319.4:c.41335C>T
(TTN)
|
NP_003310.4:p.Pro13779Ser
|
|
NM_133378.4:c.60826C>T
(TTN)
|
NP_596869.4:p.Pro20276Ser
|
|
NM_133432.3:c.41710C>T
(TTN)
|
NP_597676.3:p.Pro13904Ser
|
|
NM_133437.4:c.41911C>T
(TTN)
|
NP_597681.4:p.Pro13971Ser
|
|
NR_038271.1:n.596+6447G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-4676G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.67627C>T
(TTN)
|
XP_011510031.1:p.Pro22543Ser
|
|
XM_011511730.1:c.41521C>T
(TTN)
|
XP_011510032.1:p.Pro13841Ser
|
|
XM_011511731.1:c.41380C>T
(TTN)
|
XP_011510033.1:p.Pro13794Ser
|
|
XM_017004819.1:c.67423C>T
(TTN)
|
XP_016860308.1:p.Pro22475Ser
|
|
XM_017004820.1:c.62821C>T
(TTN)
|
XP_016860309.1:p.Pro20941Ser
|
|
XM_017004821.1:c.62818C>T
(TTN)
|
XP_016860310.1:p.Pro20940Ser
|
|
XM_017004822.1:c.59860C>T
(TTN)
|
XP_016860311.1:p.Pro19954Ser
|
|
XM_017004823.1:c.41476C>T
(TTN)
|
XP_016860312.1:p.Pro13826Ser
|
|
XM_024453094.1:c.62971C>T
(TTN)
|
XP_024308862.1:p.Pro20991Ser
|
|
XM_024453095.1:c.62968C>T
(TTN)
|
XP_024308863.1:p.Pro20990Ser
|
|
XM_024453096.1:c.62401C>T
(TTN)
|
XP_024308864.1:p.Pro20801Ser
|
|
XM_024453097.1:c.59743C>T
(TTN)
|
XP_024308865.1:p.Pro19915Ser
|
|
XM_024453098.1:c.59662C>T
(TTN)
|
XP_024308866.1:p.Pro19888Ser
|
|
XM_024453099.1:c.41425C>T
(TTN)
|
XP_024308867.1:p.Pro13809Ser
|
|
XM_024453100.1:c.31279C>T
(TTN)
|
XP_024308868.1:p.Pro10427Ser
|
|