ENST00000399503.4:c.2632G>T
MANE Select
|
ENSP00000382423.3:p.Asp878Tyr
|
|
ENST00000399503.3:c.2632G>T
|
ENSP00000382423.3:p.Asp878Tyr
|
|
NM_005921.1:c.2632G>T
|
NP_005912.1:p.Asp878Tyr
|
|
XM_005248519.3:c.2254G>T
|
XP_005248576.2:p.Asp752Tyr
|
|
XM_011543406.1:c.2377G>T
|
XP_011541708.1:p.Asp793Tyr
|
|
XM_011543407.1:c.2353G>T
|
XP_011541709.1:p.Asp785Tyr
|
|
XM_011543408.1:c.2632G>T
|
XP_011541710.1:p.Asp878Tyr
|
|
XM_017009484.1:c.2221G>T
|
XP_016864973.1:p.Asp741Tyr
|
|
XM_017009485.1:c.2143G>T
|
XP_016864974.1:p.Asp715Tyr
|
|
XR_001742068.2:n.2663G>T
|
|
|
NM_005921.2:c.2632G>T
MANE Select
|
NP_005912.1:p.Asp878Tyr
|
|