ENST00000409383.6:c.991G>C
|
ENSP00000386346.2:p.Asp331His
|
|
ENST00000519937.7:c.991G>C
MANE Select
|
ENSP00000428719.2:p.Asp331His
|
|
ENST00000393822.7:c.991G>C
|
ENSP00000377409.4:p.Asp331His
|
|
ENST00000409383.5:c.1027G>C
|
ENSP00000386346.1:p.Asp343His
|
|
ENST00000428225.5:c.968G>C
|
|
|
ENST00000491167.1:n.191G>C
|
|
|
ENST00000494165.1:c.122G>C
|
|
|
ENST00000519937.6:c.991G>C
|
ENSP00000428719.2:p.Asp331His
|
|
NM_000542.3:c.1027G>C
|
NP_000533.3:p.Asp343His
|
|
NM_198843.2:c.1027G>C
|
NP_942140.2:p.Asp343His
|
|
XM_005264487.2:c.1027G>C
|
XP_005264544.1:p.Asp343His
|
|
XM_005264488.2:c.979G>C
|
XP_005264545.2:p.Asp327His
|
|
XM_005264490.3:c.991G>C
|
XP_005264547.2:p.Asp331His
|
|
XM_005264488.4:c.979G>C
|
XP_005264545.2:p.Asp327His
|
|
XM_005264490.4:c.991G>C
|
XP_005264547.2:p.Asp331His
|
|
NM_000542.4:c.991G>C
|
NP_000533.4:p.Asp331His
|
|
NM_001367281.1:c.991G>C
|
NP_001354210.1:p.Asp331His
|
|
NM_198843.3:c.991G>C
|
NP_942140.3:p.Asp331His
|
|
NM_000542.5:c.991G>C
MANE Select
|
NP_000533.4:p.Asp331His
|
|