ENST00000342992.11:c.59918C>G
(TTN)
|
ENSP00000343764.6:p.Ala19973Gly
|
|
ENST00000342175.11:c.41003C>G
(TTN)
|
ENSP00000340554.6:p.Ala13668Gly
|
|
ENST00000359218.10:c.40802C>G
(TTN)
|
ENSP00000352154.5:p.Ala13601Gly
|
|
ENST00000342175.10:c.41003C>G
(TTN)
|
ENSP00000340554.6:p.Ala13668Gly
|
|
ENST00000342992.10:c.59918C>G
(TTN)
|
ENSP00000343764.6:p.Ala19973Gly
|
|
ENST00000359218.9:c.40802C>G
(TTN)
|
ENSP00000352154.5:p.Ala13601Gly
|
|
ENST00000460472.6:c.40427C>G
(TTN)
|
ENSP00000434586.1:p.Ala13476Gly
|
|
ENST00000589042.5:c.67622C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala22541Gly
|
|
ENST00000591111.5:c.62699C>G
(TTN)
|
ENSP00000465570.1:p.Ala20900Gly
|
|
ENST00000615779.4:c.62699C>G
(TTN)
|
ENSP00000483597.1:p.Ala20900Gly
|
|
NM_001256850.1:c.62699C>G
(TTN)
|
NP_001243779.1:p.Ala20900Gly
|
|
NM_001267550.2:c.67622C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ala22541Gly
|
|
NM_003319.4:c.40427C>G
(TTN)
|
NP_003310.4:p.Ala13476Gly
|
|
NM_133378.4:c.59918C>G
(TTN)
|
NP_596869.4:p.Ala19973Gly
|
|
NM_133432.3:c.40802C>G
(TTN)
|
NP_597676.3:p.Ala13601Gly
|
|
NM_133437.4:c.41003C>G
(TTN)
|
NP_597681.4:p.Ala13668Gly
|
|
NR_038271.1:n.596+8126G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-2997G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.66719C>G
(TTN)
|
XP_011510031.1:p.Ala22240Gly
|
|
XM_011511730.1:c.40613C>G
(TTN)
|
XP_011510032.1:p.Ala13538Gly
|
|
XM_011511731.1:c.40472C>G
(TTN)
|
XP_011510033.1:p.Ala13491Gly
|
|
XM_017004819.1:c.66515C>G
(TTN)
|
XP_016860308.1:p.Ala22172Gly
|
|
XM_017004820.1:c.61913C>G
(TTN)
|
XP_016860309.1:p.Ala20638Gly
|
|
XM_017004821.1:c.61910C>G
(TTN)
|
XP_016860310.1:p.Ala20637Gly
|
|
XM_017004822.1:c.58952C>G
(TTN)
|
XP_016860311.1:p.Ala19651Gly
|
|
XM_017004823.1:c.40568C>G
(TTN)
|
XP_016860312.1:p.Ala13523Gly
|
|
XM_024453094.1:c.62063C>G
(TTN)
|
XP_024308862.1:p.Ala20688Gly
|
|
XM_024453095.1:c.62060C>G
(TTN)
|
XP_024308863.1:p.Ala20687Gly
|
|
XM_024453096.1:c.61493C>G
(TTN)
|
XP_024308864.1:p.Ala20498Gly
|
|
XM_024453097.1:c.58835C>G
(TTN)
|
XP_024308865.1:p.Ala19612Gly
|
|
XM_024453098.1:c.58754C>G
(TTN)
|
XP_024308866.1:p.Ala19585Gly
|
|
XM_024453099.1:c.40517C>G
(TTN)
|
XP_024308867.1:p.Ala13506Gly
|
|
XM_024453100.1:c.30371C>G
(TTN)
|
XP_024308868.1:p.Ala10124Gly
|
|