ENST00000299314.12:c.3402T>G
MANE Select
|
ENSP00000299314.7:p.Val1134=
|
|
ENST00000299314.11:c.3402T>G
|
ENSP00000299314.7:p.Val1134=
|
|
ENST00000549194.1:n.268T>G
|
|
|
ENST00000549738.5:c.153T>G
|
ENSP00000450161.1:p.Val51=
|
|
ENST00000550718.1:c.214T>G
|
|
|
NM_024312.4:c.3402T>G
|
NP_077288.2:p.Val1134=
|
|
XM_006719593.2:c.3402T>G
|
XP_006719656.1:p.Val1134=
|
|
XM_011538731.1:c.3321T>G
|
XP_011537033.1:p.Val1107=
|
|
XM_006719593.3:c.3402T>G
|
XP_006719656.1:p.Val1134=
|
|
XM_011538731.2:c.3321T>G
|
XP_011537033.1:p.Val1107=
|
|
XM_017019961.1:c.3186T>G
|
XP_016875450.1:p.Val1062=
|
|
XM_017019962.2:c.2175T>G
|
XP_016875451.1:p.Val725=
|
|
NM_024312.5:c.3402T>G
MANE Select
|
NP_077288.2:p.Val1134=
|
|