ENST00000684519.1:c.418+81866T>C
MANE Select
|
ENSP00000507484.1:n.418+81866T>C
|
|
ENST00000642719.1:c.418+81866T>C
|
ENSP00000496601.1:n.418+81866T>C
|
|
ENST00000217246.8:c.418+81866T>C
|
ENSP00000217246.4:n.418+81866T>C
|
|
ENST00000463861.5:n.147+81866T>C
|
|
|
ENST00000464883.5:n.181+81866T>C
|
|
|
ENST00000497992.1:n.174+81866T>C
|
|
|
NM_080676.5:c.418+81866T>C
|
NP_542407.2:n.418+81866T>C
|
|
NM_001351661.1:c.418+81866T>C
|
NP_001338590.1:n.418+81866T>C
|
|
NM_001351663.1:c.418+81866T>C
|
NP_001338592.1:n.418+81866T>C
|
|
NM_001351661.2:c.418+81866T>C
MANE Select
|
NP_001338590.1:n.418+81866T>C
|
|
NM_001351663.2:c.418+81866T>C
|
NP_001338592.1:n.418+81866T>C
|
|
NM_080676.6:c.418+81866T>C
|
NP_542407.2:n.418+81866T>C
|
|