ENST00000339818.9:c.659T>G
MANE Select
|
ENSP00000344566.4:p.Ile220Ser
|
|
ENST00000325223.7:c.656T>G
|
ENSP00000317302.7:p.Ile219Ser
|
|
ENST00000339818.8:c.659T>G
|
ENSP00000344566.4:p.Ile220Ser
|
|
ENST00000397956.7:c.1016T>G
|
ENSP00000381047.3:p.Ile339Ser
|
|
ENST00000462742.1:n.4113T>G
|
|
|
ENST00000470196.5:n.235T>G
|
|
|
ENST00000496321.5:n.772T>G
|
|
|
NM_001271440.1:c.656T>G
|
NP_001258369.1:p.Ile219Ser
|
|
NM_001271441.1:c.1016T>G
|
NP_001258370.1:p.Ile339Ser
|
|
NM_001271442.1:c.533T>G
|
NP_001258371.1:p.Ile178Ser
|
|
NM_004928.2:c.659T>G
|
NP_004919.1:p.Ile220Ser
|
|
XM_006724051.2:c.734T>G
|
XP_006724114.1:p.Ile245Ser
|
|
XM_006724052.2:c.731T>G
|
XP_006724115.1:p.Ile244Ser
|
|
XM_006724053.2:c.335T>G
|
XP_006724116.1:p.Ile112Ser
|
|
XR_937571.1:n.1219T>G
|
|
|
XM_006724051.3:c.734T>G
|
XP_006724114.1:p.Ile245Ser
|
|
XM_006724053.3:c.335T>G
|
XP_006724116.1:p.Ile112Ser
|
|
XM_017028470.1:c.860T>G
|
XP_016883959.1:p.Ile287Ser
|
|
XM_017028471.1:c.608T>G
|
XP_016883960.1:p.Ile203Ser
|
|
XM_017028472.1:c.332T>G
|
XP_016883961.1:p.Ile111Ser
|
|
XR_937571.2:n.1226T>G
|
|
|
NM_004928.3:c.659T>G
MANE Select
|
NP_004919.1:p.Ile220Ser
|
|
NM_001271440.2:c.656T>G
|
NP_001258369.1:p.Ile219Ser
|
|
NM_001271441.2:c.1016T>G
|
NP_001258370.1:p.Ile339Ser
|
|