ENST00000261769.10:c.2351G>C
MANE Select
|
ENSP00000261769.4:p.Arg784Pro
|
|
ENST00000261769.9:c.2351G>C
|
ENSP00000261769.4:p.Arg784Pro
|
|
ENST00000422392.6:c.2168G>C
|
ENSP00000414946.2:p.Arg723Pro
|
|
ENST00000562118.1:n.569G>C
|
|
|
ENST00000562836.5:n.2422G>C
|
|
|
ENST00000566510.5:c.*1017G>C
|
ENSP00000458139.1:n.*1017G>C
|
|
ENST00000566612.5:c.*591G>C
|
ENSP00000454782.1:n.*591G>C
|
|
ENST00000611625.4:c.2414G>C
|
ENSP00000481063.1:p.Arg805Pro
|
|
ENST00000612417.4:c.1853+3155G>C
|
ENSP00000478360.1:n.1853+3155G>C
|
|
ENST00000621016.4:c.1866-4494G>C
|
ENSP00000480664.1:n.1866-4494G>C
|
|
NM_004360.3:c.2351G>C , LRG_301t1:c.2351G>C
|
NP_004351.1:p.Arg784Pro
|
|
XM_011523488.1:c.1616G>C
|
XP_011521790.1:p.Arg539Pro
|
|
XM_011523489.1:c.1616G>C
|
XP_011521791.1:p.Arg539Pro
|
|
NM_001317184.1:c.2168G>C
|
NP_001304113.1:p.Arg723Pro
|
|
NM_001317185.1:c.803G>C
|
NP_001304114.1:p.Arg268Pro
|
|
NM_001317186.1:c.386G>C
|
NP_001304115.1:p.Arg129Pro
|
|
NM_004360.4:c.2351G>C
|
NP_004351.1:p.Arg784Pro
|
|
NM_004360.5:c.2351G>C
MANE Select
|
NP_004351.1:p.Arg784Pro
|
|
NM_001317184.2:c.2168G>C
|
NP_001304113.1:p.Arg723Pro
|
|
NM_001317185.2:c.803G>C
|
NP_001304114.1:p.Arg268Pro
|
|
NM_001317186.2:c.386G>C
|
NP_001304115.1:p.Arg129Pro
|
|