ENST00000330342.8:c.1327-7T>C
MANE Select
|
ENSP00000332247.2:n.1327-7T>C
|
|
ENST00000540368.6:n.1358-7T>C
|
|
|
ENST00000674794.1:c.1415-7T>C
|
|
|
ENST00000675260.1:n.602-7T>C
|
|
|
ENST00000675344.1:c.*348-7T>C
|
ENSP00000501953.1:n.*348-7T>C
|
|
ENST00000330342.7:c.1327-7T>C
|
ENSP00000332247.2:n.1327-7T>C
|
|
ENST00000504192.2:c.937-7T>C
|
ENSP00000443441.1:n.937-7T>C
|
|
ENST00000536426.1:n.344-7T>C
|
|
|
ENST00000545059.5:n.3963-7T>C
|
|
|
NM_012463.3:c.1327-7T>C
|
NP_036595.2:n.1327-7T>C
|
|
XM_005253563.1:c.1327-7T>C
|
XP_005253620.1:n.1327-7T>C
|
|
XM_006719317.2:c.814-7T>C
|
XP_006719380.1:n.814-7T>C
|
|
XM_006719318.2:c.505-7T>C
|
XP_006719381.1:n.505-7T>C
|
|
XR_429088.1:n.1490-7T>C
|
|
|
XM_024448910.1:c.1327-7T>C
|
XP_024304678.1:n.1327-7T>C
|
|
XM_024448911.1:c.814-7T>C
|
XP_024304679.1:n.814-7T>C
|
|
XM_024448912.1:c.505-7T>C
|
XP_024304680.1:n.505-7T>C
|
|
NM_012463.4:c.1327-7T>C
MANE Select
|
NP_036595.2:n.1327-7T>C
|
|