ENST00000326637.8:c.1772+31526T>G
(TNNI3K)
MANE Select
|
ENSP00000322251.3:n.1772+31526T>G
|
|
ENST00000557284.7:c.2075+31526T>G
(FPGT-TNNI3K)
|
ENSP00000450895.3:n.2075+31526T>G
|
|
ENST00000648585.1:c.*1678+31526T>G
(FPGT-TNNI3K)
|
ENSP00000497631.1:n.*1678+31526T>G
|
|
ENST00000326637.7:c.1772+31526T>G
(TNNI3K)
|
ENSP00000322251.3:n.1772+31526T>G
|
|
ENST00000370899.7:c.2075+31526T>G
(FPGT-TNNI3K)
|
ENSP00000359936.3:n.2075+31526T>G
|
|
ENST00000525480.2:c.332-16250T>G
(TNNI3K)
|
|
|
ENST00000534020.5:c.424T>G
(TNNI3K)
|
ENSP00000434975.1:p.Cys142Gly
|
|
ENST00000557284.6:c.2114+31526T>G
(FPGT-TNNI3K)
|
ENSP00000450895.2:n.2114+31526T>G
|
|
NM_001112808.2:c.2114+31526T>G
(FPGT-TNNI3K)
|
NP_001106279.2:n.2114+31526T>G
|
|
NM_001199327.1:c.2114+31526T>G
(FPGT-TNNI3K)
|
NP_001186256.2:n.2114+31526T>G
|
|
NM_015978.2:c.1772+31526T>G
(TNNI3K)
|
NP_057062.1:n.1772+31526T>G
|
|
NM_015978.3:c.1772+31526T>G
(TNNI3K)
MANE Select
|
NP_057062.1:n.1772+31526T>G
|
|
NM_001112808.3:c.2075+31526T>G
(FPGT-TNNI3K)
|
NP_001106279.3:n.2075+31526T>G
|
|
NM_001199327.2:c.2075+31526T>G
(FPGT-TNNI3K)
|
NP_001186256.3:n.2075+31526T>G
|
|