ENST00000217381.3:c.496+180G>C
MANE Select
|
ENSP00000217381.2:n.496+180G>C
|
|
ENST00000217381.2:c.496+180G>C
|
ENSP00000217381.2:n.496+180G>C
|
|
NM_003098.2:c.496+180G>C , LRG_332t1:c.496+180G>C
|
NP_003089.1:n.496+180G>C
|
|
XM_005260517.1:c.496+180G>C
|
XP_005260574.1:n.496+180G>C
|
|
XM_011529007.1:c.496+180G>C
|
XP_011527309.1:n.496+180G>C
|
|
XM_011529008.1:c.496+180G>C
|
XP_011527310.1:n.496+180G>C
|
|
XR_936612.1:n.729+180G>C
|
|
|
XM_024451971.1:c.169+180G>C
|
XP_024307739.1:n.169+180G>C
|
|
NM_003098.3:c.496+180G>C
MANE Select
|
NP_003089.1:n.496+180G>C
|
|