ENST00000493477.2:n.1689G>T
|
|
|
ENST00000682162.1:c.1215G>T
|
ENSP00000508203.1:n.1215G>T
|
|
ENST00000682567.1:n.2734G>T
|
|
|
ENST00000683521.1:c.1186G>T
|
ENSP00000506864.1:p.Val396Phe
|
|
ENST00000684161.1:n.2401G>T
|
|
|
ENST00000684483.1:c.*582G>T
|
ENSP00000507894.1:n.*582G>T
|
|
ENST00000366560.4:c.1186G>T
MANE Select
|
ENSP00000355518.4:p.Val396Phe
|
|
ENST00000366560.3:c.1186G>T
|
ENSP00000355518.3:p.Val396Phe
|
|
NM_000143.3:c.1186G>T , LRG_504t1:c.1186G>T
|
NP_000134.2:p.Val396Phe
|
|
XM_011544132.1:c.958G>T
|
XP_011542434.1:p.Val320Phe
|
|
XM_011544132.2:c.958G>T
|
XP_011542434.1:p.Val320Phe
|
|
NM_000143.4:c.1186G>T
MANE Select
|
NP_000134.2:p.Val396Phe
|
|