ENST00000316386.11:c.40C>T
MANE Select
|
ENSP00000319476.6:p.Arg14Cys
|
|
ENST00000316386.10:c.40C>T
|
ENSP00000319476.6:p.Arg14Cys
|
|
ENST00000435193.1:c.40C>T
|
ENSP00000415951.1:p.Arg14Cys
|
|
NM_012092.3:c.40C>T , LRG_65t1:c.40C>T
|
NP_036224.1:p.Arg14Cys
|
|
XM_011511028.1:c.40C>T
|
XP_011509330.1:p.Arg14Cys
|
|
XM_011511030.1:c.-378C>T
|
XP_011509332.1:n.-378C>T
|
|
XM_011511031.1:c.-282C>T
|
XP_011509333.1:n.-282C>T
|
|
XR_427213.2:n.366+463G>A
|
|
|
XR_001739861.1:n.380+463G>A
|
|
|
XR_427213.3:n.380+463G>A
|
|
|
NM_012092.4:c.40C>T
MANE Select
|
NP_036224.1:p.Arg14Cys
|
|