|
NM_033200.3:c.311A>G
MANE Select
|
NP_149977.2:p.Tyr104Cys
|
|
ENST00000474879.7:c.311A>G
MANE Select
|
ENSP00000424381.1:p.Tyr104Cys
|
|
NM_001363816.1:c.236A>G
|
NP_001350745.1:p.Tyr79Cys
|
|
NM_001363816.2:c.236A>G
|
NP_001350745.1:p.Tyr79Cys
|
|
NM_033200.2:c.311A>G
|
NP_149977.2:p.Tyr104Cys
|
|
ENST00000216080.5:c.236A>G
|
ENSP00000216080.5:p.Tyr79Cys
|
|
ENST00000474879.6:c.311A>G
|
ENSP00000424381.1:p.Tyr104Cys
|
|
ENST00000505981.5:n.241A>G
|
|
|
ENST00000507607.1:n.432A>G
|
|
|
XM_005261955.2:c.236A>G
|
XP_005262012.1:p.Tyr79Cys
|
|
XM_006724426.2:c.231A>G
|
XP_006724489.1:p.Leu77=
|
|
XM_006724426.3:c.231A>G
|
XP_006724489.1:p.Leu77=
|
|
XM_006724427.2:c.231A>G
|
XP_006724490.1:p.Leu77=
|
|
XM_006724427.3:c.231A>G
|
XP_006724490.1:p.Leu77=
|
|
XM_017029077.2:c.311A>G
|
XP_016884566.1:p.Tyr104Cys
|
|
XR_001755368.2:n.417A>G
|
|
|
XR_938349.1:n.476A>G
|
|
|
XR_938349.3:n.417A>G
|
|