ENST00000451389.7:c.247A>G
|
ENSP00000508581.1:p.Ile83Val
|
|
ENST00000507563.7:c.189A>G
|
ENSP00000510363.1:p.Ser63=
|
|
ENST00000540194.6:n.1006A>G
|
|
|
ENST00000542946.2:c.247A>G
|
ENSP00000445792.1:p.Ile83Val
|
|
ENST00000543594.6:c.*458A>G
|
ENSP00000509354.1:n.*458A>G
|
|
ENST00000685597.1:c.247A>G
|
ENSP00000509403.1:p.Ile83Val
|
|
ENST00000686820.1:c.189A>G
|
ENSP00000508587.1:p.Ser63=
|
|
ENST00000688279.1:c.189A>G
|
ENSP00000510422.1:p.Ser63=
|
|
ENST00000688430.1:n.173A>G
|
|
|
ENST00000689076.1:c.247A>G
|
ENSP00000508469.1:p.Ile83Val
|
|
ENST00000689882.1:c.189A>G
|
ENSP00000509351.1:p.Ser63=
|
|
ENST00000691720.1:c.247A>G
|
ENSP00000509146.1:p.Ile83Val
|
|
ENST00000692219.1:c.247A>G
|
ENSP00000510149.1:p.Ile83Val
|
|
ENST00000692667.1:c.247A>G
|
ENSP00000510180.1:p.Ile83Val
|
|
ENST00000692785.1:c.247A>G
|
ENSP00000509310.1:p.Ile83Val
|
|
ENST00000693557.1:c.247A>G
|
ENSP00000508970.1:p.Ile83Val
|
|
ENST00000278826.11:c.247A>G
MANE Select
|
ENSP00000278826.5:p.Ile83Val
|
|
ENST00000278826.10:c.247A>G
|
ENSP00000278826.5:p.Ile83Val
|
|
ENST00000381787.2:c.73A>G
|
ENSP00000371206.2:p.Ile25Val
|
|
ENST00000423772.6:n.1766A>G
|
|
|
ENST00000451389.6:n.388A>G
|
|
|
ENST00000507563.6:n.420A>G
|
|
|
ENST00000534963.5:n.346A>G
|
|
|
ENST00000540194.5:n.421A>G
|
|
|
ENST00000542946.1:c.247A>G
|
ENSP00000445792.1:p.Ile83Val
|
|
ENST00000545420.1:n.271A>G
|
|
|
NM_016464.4:c.247A>G
|
NP_057548.1:p.Ile83Val
|
|
NR_028473.1:n.689A>G
|
|
|
XM_006718585.2:c.247A>G
|
XP_006718648.1:p.Ile83Val
|
|
XM_006718586.1:c.247A>G
|
XP_006718649.1:p.Ile83Val
|
|
XM_006718588.2:c.73A>G
|
XP_006718651.1:p.Ile25Val
|
|
XM_011545098.1:c.247A>G
|
XP_011543400.1:p.Ile83Val
|
|
XM_011545099.1:c.247A>G
|
XP_011543401.1:p.Ile83Val
|
|
XM_011545100.1:c.247A>G
|
XP_011543402.1:p.Ile83Val
|
|
XR_949964.1:n.446A>G
|
|
|
XR_949965.1:n.446A>G
|
|
|
XR_949966.1:n.446A>G
|
|
|
NM_001330281.1:c.73A>G
|
NP_001317210.1:p.Ile25Val
|
|
XM_006718585.3:c.247A>G
|
XP_006718648.1:p.Ile83Val
|
|
XM_006718586.2:c.247A>G
|
XP_006718649.1:p.Ile83Val
|
|
XM_011545098.2:c.247A>G
|
XP_011543400.1:p.Ile83Val
|
|
XM_011545099.2:c.247A>G
|
XP_011543401.1:p.Ile83Val
|
|
XM_017017917.1:c.247A>G
|
XP_016873406.1:p.Ile83Val
|
|
XR_949964.3:n.446A>G
|
|
|
XR_949966.2:n.446A>G
|
|
|
NM_016464.5:c.247A>G
MANE Select
|
NP_057548.1:p.Ile83Val
|
|
NM_001330281.2:c.73A>G
|
NP_001317210.1:p.Ile25Val
|
|
NR_028473.2:n.316A>G
|
|
|