ENST00000330342.8:c.732-1G>C
MANE Select
|
ENSP00000332247.2:n.732-1G>C
|
|
ENST00000540368.6:n.763-1G>C
|
|
|
ENST00000613625.5:c.732-1G>C
|
ENSP00000482236.1:n.732-1G>C
|
|
ENST00000674794.1:c.172-1G>C
|
|
|
ENST00000675344.1:c.732-1G>C
|
ENSP00000501953.1:n.732-1G>C
|
|
ENST00000330342.7:c.732-1G>C
|
ENSP00000332247.2:n.732-1G>C
|
|
ENST00000504192.2:c.342-1G>C
|
ENSP00000443441.1:n.342-1G>C
|
|
ENST00000540368.5:n.942-1G>C
|
|
|
ENST00000545059.5:n.3368-1G>C
|
|
|
ENST00000613625.4:c.732-1G>C
|
ENSP00000482236.1:n.732-1G>C
|
|
NM_012463.3:c.732-1G>C
|
NP_036595.2:n.732-1G>C
|
|
XM_005253563.1:c.732-1G>C
|
XP_005253620.1:n.732-1G>C
|
|
XM_006719317.2:c.219-1G>C
|
XP_006719380.1:n.219-1G>C
|
|
XR_429088.1:n.895-1G>C
|
|
|
XM_024448910.1:c.732-1G>C
|
XP_024304678.1:n.732-1G>C
|
|
XM_024448911.1:c.219-1G>C
|
XP_024304679.1:n.219-1G>C
|
|
NM_012463.4:c.732-1G>C
MANE Select
|
NP_036595.2:n.732-1G>C
|
|