ENST00000262461.7:c.3598G>T
MANE Select
|
ENSP00000262461.2:p.Val1200Phe
|
|
ENST00000262461.6:c.3598G>T
|
ENSP00000262461.2:p.Val1200Phe
|
|
ENST00000343225.4:c.3550G>T
|
ENSP00000340878.4:p.Val1184Phe
|
|
ENST00000509205.5:c.*211G>T
|
ENSP00000427109.1:n.*211G>T
|
|
NM_001046.2:c.3598G>T
|
NP_001037.1:p.Val1200Phe
|
|
NM_001256461.1:c.3550G>T
|
NP_001243390.1:p.Val1184Phe
|
|
NR_046207.1:n.3828G>T
|
|
|
XM_017009771.1:c.1840G>T
|
XP_016865260.1:p.Val614Phe
|
|
XR_001742214.1:n.3822G>T
|
|
|
NM_001046.3:c.3598G>T
MANE Select
|
NP_001037.1:p.Val1200Phe
|
|
NM_001256461.2:c.3550G>T
|
NP_001243390.1:p.Val1184Phe
|
|
NR_046207.2:n.3853G>T
|
|
|