ENST00000696809.1:c.*1488A=
|
ENSP00000512887.1:n.*1488A=
|
|
ENST00000699276.1:c.*542A=
|
ENSP00000514257.1:n.*542A=
|
|
ENST00000323584.10:c.2914A=
MANE Select
|
ENSP00000313504.5:p.Met972=
|
|
ENST00000299167.12:c.2914A=
|
ENSP00000299167.8:p.Met972=
|
|
ENST00000323584.9:c.2914A=
|
ENSP00000313504.5:p.Met972=
|
|
ENST00000566044.5:c.2893A=
|
ENSP00000456729.1:p.Met965=
|
|
ENST00000566319.2:n.1730A=
|
|
|
NM_000293.2:c.2914A=
|
NP_000284.1:p.Met972=
|
|
NM_001031835.2:c.2893A=
|
NP_001027005.1:p.Met965=
|
|
XM_005255983.3:c.2914A=
|
XP_005256040.1:p.Met972=
|
|
XM_005255984.3:c.2893A=
|
XP_005256041.1:p.Met965=
|
|
XM_011523107.1:c.1492A=
|
XP_011521409.1:p.Met498=
|
|
NM_001363837.1:c.2914A=
|
NP_001350766.1:p.Met972=
|
|
XM_005255983.4:c.2914A=
|
XP_005256040.1:p.Met972=
|
|
XM_005255984.4:c.2893A=
|
XP_005256041.1:p.Met965=
|
|
XM_017023282.1:c.1801A=
|
XP_016878771.1:p.Met601=
|
|
XM_017023283.1:c.1492A=
|
XP_016878772.1:p.Met498=
|
|
XM_017023284.1:c.1492A=
|
XP_016878773.1:p.Met498=
|
|
XR_001751913.1:n.2838A=
|
|
|
NM_000293.3:c.2914A=
MANE Select
|
NP_000284.1:p.Met972=
|
|
NM_001031835.3:c.2893A=
|
NP_001027005.1:p.Met965=
|
|