|
NM_004312.3:c.298C>T
MANE Select
|
NP_004303.2:p.Arg100Ter
|
|
ENST00000307959.9:c.298C>T
MANE Select
|
ENSP00000311538.8:p.Arg100Ter
|
|
NM_004312.2:c.298C>T
|
NP_004303.2:p.Arg100Ter
|
|
ENST00000307959.8:c.298C>T
|
ENSP00000311538.8:p.Arg100Ter
|
|
ENST00000374495.7:c.298C>T
|
ENSP00000363619.3:p.Arg100Ter
|
|
ENST00000480877.6:c.145C>T
|
ENSP00000425505.1:p.Arg49Ter
|
|
ENST00000620997.4:c.298C>T
|
ENSP00000480426.1:p.Arg100Ter
|
|
XM_011530956.1:c.412C>T
|
XP_011529258.1:p.Arg138Ter
|
|
XM_017029518.1:c.343C>T
|
XP_016885007.1:p.Arg115Ter
|
|
XR_938428.1:n.503+4516G>A
|
|
|
XR_938429.1:n.503+4516G>A
|
|