|
ENST00000710359.1:c.5790A>T
|
ENSP00000518230.1:p.Ala1930=
|
|
|
ENST00000379802.8:c.7119A>T
MANE Select
|
ENSP00000369129.3:p.Ala2373=
|
|
|
ENST00000379802.7:c.7119A>T
|
ENSP00000369129.3:p.Ala2373=
|
|
|
ENST00000418664.2:c.5322A>T
|
ENSP00000396591.2:p.Ala1774=
|
|
|
NM_001008844.1:c.5322A>T
|
NP_001008844.1:p.Ala1774=
|
|
|
NM_004415.2:c.7119A>T , LRG_423t1:c.7119A>T
|
NP_004406.2:p.Ala2373=
|
|
|
XM_011514323.1:c.5790A>T
|
XP_011512625.1:p.Ala1930=
|
|
|
NM_001008844.2:c.5322A>T
|
NP_001008844.1:p.Ala1774=
|
|
|
NM_001319034.1:c.5790A>T
|
NP_001305963.1:p.Ala1930=
|
|
|
NM_004415.3:c.7119A>T
|
NP_004406.2:p.Ala2373=
|
|
|
NM_004415.4:c.7119A>T
MANE Select
|
NP_004406.2:p.Ala2373=
|
|
|
NM_001008844.3:c.5322A>T
|
NP_001008844.1:p.Ala1774=
|
|
|
NM_001319034.2:c.5790A>T
|
NP_001305963.1:p.Ala1930=
|
|
