ENST00000346342.8:c.1168T>C
MANE Select
|
ENSP00000329546.4:p.Tyr390His
|
|
ENST00000346342.7:c.1168T>C
|
ENSP00000329546.3:p.Tyr390His
|
|
ENST00000375581.3:c.1234T>C
|
ENSP00000364731.3:p.Tyr412His
|
|
ENST00000541084.5:c.982T>C
|
ENSP00000442051.2:p.Tyr328His
|
|
NM_000131.4:c.1234T>C , LRG_554t1:c.1234T>C
|
NP_000122.1:p.Tyr412His
|
|
NM_001267554.1:c.982T>C
|
NP_001254483.1:p.Tyr328His
|
|
NM_019616.3:c.1168T>C , LRG_554t2:c.1168T>C
|
NP_062562.1:p.Tyr390His
|
|
NR_051961.1:n.1255T>C
|
|
|
XM_006719963.2:c.1027T>C
|
XP_006720026.1:p.Tyr343His
|
|
XM_011537474.1:c.1276T>C
|
XP_011535776.1:p.Tyr426His
|
|
XM_011537475.1:c.1090T>C
|
XP_011535777.1:p.Tyr364His
|
|
XM_011537476.1:c.928T>C
|
XP_011535778.1:p.Tyr310His
|
|
XM_011537477.1:c.1237T>C
|
XP_011535779.1:p.Tyr413His
|
|
XM_006719963.3:c.1072T>C
|
XP_006720026.2:p.Tyr358His
|
|
XM_011537474.2:c.1321T>C
|
XP_011535776.2:p.Tyr441His
|
|
XM_011537475.2:c.1135T>C
|
XP_011535777.2:p.Tyr379His
|
|
XM_011537476.2:c.928T>C
|
XP_011535778.1:p.Tyr310His
|
|
NM_019616.4:c.1168T>C
MANE Select
|
NP_062562.1:p.Tyr390His
|
|
NR_051961.2:n.1252T>C
|
|
|
NM_001267554.2:c.982T>C
|
NP_001254483.1:p.Tyr328His
|
|