ENST00000697603.1:c.2198A>G
|
ENSP00000513358.1:p.Asp733Gly
|
|
ENST00000697607.1:n.1053A>G
|
|
|
ENST00000314191.7:c.9521A>G
MANE Select
|
ENSP00000313420.3:p.Asp3174Gly
|
|
ENST00000314191.6:c.9521A>G
|
ENSP00000313420.3:p.Asp3174Gly
|
|
ENST00000338368.7:c.9521A>G
|
ENSP00000345182.4:p.Asp3174Gly
|
|
NM_001081640.1:c.9521A>G
|
NP_001075109.1:p.Asp3174Gly
|
|
NM_006904.6:c.9521A>G , LRG_162t1:c.9521A>G
|
NP_008835.5:p.Asp3174Gly
|
|
XM_011517567.1:c.9524A>G
|
XP_011515869.1:p.Asp3175Gly
|
|
XM_011517568.1:c.9524A>G
|
XP_011515870.1:p.Asp3175Gly
|
|
NM_001081640.2:c.9521A>G
|
NP_001075109.1:p.Asp3174Gly
|
|
NM_006904.7:c.9521A>G
MANE Select
|
NP_008835.5:p.Asp3174Gly
|
|