ENST00000399408.7:c.4051T>G
|
ENSP00000382340.4:p.Phe1351Val
|
|
ENST00000399410.8:c.4021T>G
MANE Select
|
ENSP00000382342.3:p.Phe1341Val
|
|
ENST00000572882.3:c.3844T>G
|
ENSP00000461615.2:p.Phe1282Val
|
|
ENST00000676806.1:n.747T>G
|
|
|
ENST00000677164.1:c.3550T>G
|
ENSP00000502873.1:p.Phe1184Val
|
|
ENST00000678422.1:c.*1313T>G
|
ENSP00000503954.1:n.*1313T>G
|
|
ENST00000399408.6:c.3073T>G
|
ENSP00000382340.3:p.Phe1025Val
|
|
ENST00000399410.7:c.4021T>G
|
ENSP00000382342.3:p.Phe1341Val
|
|
ENST00000572882.2:c.3746T>G
|
|
|
NM_004996.3:c.4021T>G
|
NP_004987.2:p.Phe1341Val
|
|
XM_011522497.1:c.3997T>G
|
XP_011520799.1:p.Phe1333Val
|
|
XM_011522498.1:c.3928T>G
|
XP_011520800.1:p.Phe1310Val
|
|
XM_011522498.2:c.3928T>G
|
XP_011520800.1:p.Phe1310Val
|
|
XM_017023237.1:c.4075T>G
|
XP_016878726.1:p.Phe1359Val
|
|
XM_017023238.1:c.3949T>G
|
XP_016878727.1:p.Phe1317Val
|
|
XM_017023239.1:c.3937T>G
|
XP_016878728.1:p.Phe1313Val
|
|
XM_017023240.1:c.3898T>G
|
XP_016878729.1:p.Phe1300Val
|
|
XM_017023241.1:c.3811T>G
|
XP_016878730.1:p.Phe1271Val
|
|
XM_017023242.1:c.3730T>G
|
XP_016878731.1:p.Phe1244Val
|
|
NM_004996.4:c.4021T>G
MANE Select
|
NP_004987.2:p.Phe1341Val
|
|