ENST00000342992.11:c.52237C>G
(TTN)
|
ENSP00000343764.6:p.Pro17413Ala
|
|
ENST00000342175.11:c.33322C>G
(TTN)
|
ENSP00000340554.6:p.Pro11108Ala
|
|
ENST00000359218.10:c.33121C>G
(TTN)
|
ENSP00000352154.5:p.Pro11041Ala
|
|
ENST00000342175.10:c.33322C>G
(TTN)
|
ENSP00000340554.6:p.Pro11108Ala
|
|
ENST00000342992.10:c.52237C>G
(TTN)
|
ENSP00000343764.6:p.Pro17413Ala
|
|
ENST00000359218.9:c.33121C>G
(TTN)
|
ENSP00000352154.5:p.Pro11041Ala
|
|
ENST00000460472.6:c.32746C>G
(TTN)
|
ENSP00000434586.1:p.Pro10916Ala
|
|
ENST00000589042.5:c.59941C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19981Ala
|
|
ENST00000591111.5:c.55018C>G
(TTN)
|
ENSP00000465570.1:p.Pro18340Ala
|
|
ENST00000615779.4:c.55018C>G
(TTN)
|
ENSP00000483597.1:p.Pro18340Ala
|
|
NM_001256850.1:c.55018C>G
(TTN)
|
NP_001243779.1:p.Pro18340Ala
|
|
NM_001267550.2:c.59941C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19981Ala
|
|
NM_003319.4:c.32746C>G
(TTN)
|
NP_003310.4:p.Pro10916Ala
|
|
NM_133378.4:c.52237C>G
(TTN)
|
NP_596869.4:p.Pro17413Ala
|
|
NM_133432.3:c.33121C>G
(TTN)
|
NP_597676.3:p.Pro11041Ala
|
|
NM_133437.4:c.33322C>G
(TTN)
|
NP_597681.4:p.Pro11108Ala
|
|
NR_038271.1:n.597-5718G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+564G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.59038C>G
(TTN)
|
XP_011510031.1:p.Pro19680Ala
|
|
XM_011511730.1:c.32932C>G
(TTN)
|
XP_011510032.1:p.Pro10978Ala
|
|
XM_011511731.1:c.32791C>G
(TTN)
|
XP_011510033.1:p.Pro10931Ala
|
|
XM_017004819.1:c.58834C>G
(TTN)
|
XP_016860308.1:p.Pro19612Ala
|
|
XM_017004820.1:c.54232C>G
(TTN)
|
XP_016860309.1:p.Pro18078Ala
|
|
XM_017004821.1:c.54229C>G
(TTN)
|
XP_016860310.1:p.Pro18077Ala
|
|
XM_017004822.1:c.51271C>G
(TTN)
|
XP_016860311.1:p.Pro17091Ala
|
|
XM_017004823.1:c.32887C>G
(TTN)
|
XP_016860312.1:p.Pro10963Ala
|
|
XM_024453094.1:c.54382C>G
(TTN)
|
XP_024308862.1:p.Pro18128Ala
|
|
XM_024453095.1:c.54379C>G
(TTN)
|
XP_024308863.1:p.Pro18127Ala
|
|
XM_024453096.1:c.53812C>G
(TTN)
|
XP_024308864.1:p.Pro17938Ala
|
|
XM_024453097.1:c.51154C>G
(TTN)
|
XP_024308865.1:p.Pro17052Ala
|
|
XM_024453098.1:c.51073C>G
(TTN)
|
XP_024308866.1:p.Pro17025Ala
|
|
XM_024453099.1:c.32836C>G
(TTN)
|
XP_024308867.1:p.Pro10946Ala
|
|
XM_024453100.1:c.22690C>G
(TTN)
|
XP_024308868.1:p.Pro7564Ala
|
|