ENST00000354393.7:c.2333G>A
|
ENSP00000346369.2:p.Arg778Lys
|
|
ENST00000540630.6:c.3212G>A
|
ENSP00000441668.3:p.Arg1071Lys
|
|
ENST00000613327.5:c.3158G>A
|
ENSP00000480757.2:p.Arg1053Lys
|
|
ENST00000688812.1:c.*421G>A
|
ENSP00000510658.1:n.*421G>A
|
|
ENST00000690544.1:c.*2429G>A
|
ENSP00000508989.1:n.*2429G>A
|
|
ENST00000358913.10:c.3158G>A
MANE Select
|
ENSP00000351790.5:p.Arg1053Lys
|
|
ENST00000354393.6:c.2333G>A
|
ENSP00000346369.2:p.Arg778Lys
|
|
ENST00000358913.9:c.3158G>A
|
ENSP00000351790.5:p.Arg1053Lys
|
|
ENST00000540630.5:c.3158G>A
|
ENSP00000441668.2:p.Arg1053Lys
|
|
ENST00000613327.4:c.2276G>A
|
ENSP00000480757.1:p.Arg759Lys
|
|
NM_001256267.1:c.3158G>A
|
NP_001243196.1:p.Arg1053Lys
|
|
NM_001256268.1:c.2276G>A
|
NP_001243197.1:p.Arg759Lys
|
|
NM_032578.3:c.3158G>A , LRG_410t1:c.3158G>A
|
NP_115967.2:p.Arg1053Lys
|
|
NR_045662.3:n.2585G>A
|
|
|
NR_045663.3:n.3287G>A
|
|
|
XM_006718043.2:c.3212G>A
|
XP_006718106.1:p.Arg1071Lys
|
|
XM_011540292.1:c.3188G>A
|
XP_011538594.1:p.Arg1063Lys
|
|
XM_017016833.1:c.3236G>A
|
XP_016872322.1:p.Arg1079Lys
|
|
XM_017016834.2:c.3158G>A
|
XP_016872323.1:p.Arg1053Lys
|
|
XM_024448236.1:c.2036G>A
|
XP_024304004.1:p.Arg679Lys
|
|
NR_045662.4:n.2695G>A
|
|
|
NR_045663.4:n.3232G>A
|
|
|
NM_001256267.2:c.3158G>A
|
NP_001243196.1:p.Arg1053Lys
|
|
NM_001256268.2:c.2276G>A
|
NP_001243197.1:p.Arg759Lys
|
|
NM_032578.4:c.3158G>A
MANE Select
|
NP_115967.2:p.Arg1053Lys
|
|