ENST00000296782.10:c.2545G>C
|
ENSP00000296782.5:p.Glu849Gln
|
|
ENST00000503698.2:c.505G>C
|
ENSP00000518563.1:p.Glu169Gln
|
|
ENST00000514735.2:c.2497G>C
|
ENSP00000423162.2:p.Glu833Gln
|
|
ENST00000711063.1:c.2545G>C
|
ENSP00000518562.1:p.Glu849Gln
|
|
ENST00000357387.8:c.2545G>C
MANE Select
|
ENSP00000349959.3:p.Glu849Gln
|
|
ENST00000296782.9:c.2545G>C
|
ENSP00000296782.5:p.Glu849Gln
|
|
ENST00000357387.7:c.2545G>C
|
ENSP00000349959.3:p.Glu849Gln
|
|
ENST00000503698.1:n.505G>C
|
|
|
ENST00000511516.5:c.*1769G>C
|
ENSP00000423019.1:n.*1769G>C
|
|
NM_001285439.1:c.2545G>C
|
NP_001272368.1:p.Glu849Gln
|
|
NM_001285440.1:c.1690G>C
|
NP_001272369.1:p.Glu564Gln
|
|
NM_152756.4:c.2545G>C
|
NP_689969.2:p.Glu849Gln
|
|
XM_006714463.2:c.2545G>C
|
XP_006714526.1:p.Glu849Gln
|
|
XM_011514005.1:c.2545G>C
|
XP_011512307.1:p.Glu849Gln
|
|
XM_011514006.1:c.2356G>C
|
XP_011512308.1:p.Glu786Gln
|
|
XM_011514007.1:c.1690G>C
|
XP_011512309.1:p.Glu564Gln
|
|
XM_006714463.3:c.2545G>C
|
XP_006714526.1:p.Glu849Gln
|
|
XM_011514005.2:c.2545G>C
|
XP_011512307.1:p.Glu849Gln
|
|
XM_011514006.3:c.2356G>C
|
XP_011512308.1:p.Glu786Gln
|
|
XM_017009311.1:c.2497G>C
|
XP_016864800.1:p.Glu833Gln
|
|
XM_017009312.1:c.2497G>C
|
XP_016864801.1:p.Glu833Gln
|
|
XM_017009313.1:c.2386G>C
|
XP_016864802.1:p.Glu796Gln
|
|
XM_017009314.2:c.1690G>C
|
XP_016864803.1:p.Glu564Gln
|
|
XM_017009315.2:c.1690G>C
|
XP_016864804.1:p.Glu564Gln
|
|
NM_152756.5:c.2545G>C
MANE Select
|
NP_689969.2:p.Glu849Gln
|
|
NM_001285439.2:c.2545G>C
|
NP_001272368.1:p.Glu849Gln
|
|
NM_001285440.2:c.1690G>C
|
NP_001272369.1:p.Glu564Gln
|
|