ENST00000341947.7:c.3691-129T>C
MANE Select
|
ENSP00000339915.2:n.3691-129T>C
|
|
ENST00000341947.6:c.3691-129T>C
|
ENSP00000339915.2:n.3691-129T>C
|
|
ENST00000361917.5:c.3370-129T>C
|
ENSP00000355123.1:n.3370-129T>C
|
|
ENST00000374708.8:c.3433-129T>C
|
ENSP00000363840.4:n.3433-129T>C
|
|
ENST00000477772.1:n.273-3803T>C
|
|
|
NM_080679.2:c.3370-129T>C
|
NP_542410.2:n.3370-129T>C
|
|
NM_080680.2:c.3691-129T>C
|
NP_542411.2:n.3691-129T>C
|
|
NM_080681.2:c.3433-129T>C
|
NP_542412.2:n.3433-129T>C
|
|
XM_011514298.1:c.2845-129T>C
|
XP_011512600.1:n.2845-129T>C
|
|
XM_011514299.1:c.2977-129T>C
|
XP_011512601.1:n.2977-129T>C
|
|
XM_011514300.1:c.2797-129T>C
|
XP_011512602.1:n.2797-129T>C
|
|
XM_011514301.1:c.2734-129T>C
|
XP_011512603.1:n.2734-129T>C
|
|
XM_011514302.1:c.2578-129T>C
|
XP_011512604.1:n.2578-129T>C
|
|
XM_011514299.2:c.2977-129T>C
|
XP_011512601.1:n.2977-129T>C
|
|
XM_011514300.2:c.2797-129T>C
|
XP_011512602.1:n.2797-129T>C
|
|
XM_011514302.2:c.2578-129T>C
|
XP_011512604.1:n.2578-129T>C
|
|
XM_017010250.1:c.3691-129T>C
|
XP_016865739.1:n.3691-129T>C
|
|
XM_017010251.2:c.2509-129T>C
|
XP_016865740.1:n.2509-129T>C
|
|
NM_080680.3:c.3691-129T>C
MANE Select
|
NP_542411.2:n.3691-129T>C
|
|
NM_080681.3:c.3433-129T>C
|
NP_542412.2:n.3433-129T>C
|
|
NM_080679.3:c.3370-129T>C
|
NP_542410.2:n.3370-129T>C
|
|