ENST00000683572.1:n.719C>G
|
|
|
ENST00000341947.7:c.4913C>G
MANE Select
|
ENSP00000339915.2:p.Thr1638Ser
|
|
ENST00000341947.6:c.4913C>G
|
ENSP00000339915.2:p.Thr1638Ser
|
|
ENST00000361917.5:c.4592C>G
|
ENSP00000355123.1:p.Thr1531Ser
|
|
ENST00000374708.8:c.4655C>G
|
ENSP00000363840.4:p.Thr1552Ser
|
|
ENST00000477772.1:n.703C>G
|
|
|
NM_080679.2:c.4592C>G
|
NP_542410.2:p.Thr1531Ser
|
|
NM_080680.2:c.4913C>G
|
NP_542411.2:p.Thr1638Ser
|
|
NM_080681.2:c.4655C>G
|
NP_542412.2:p.Thr1552Ser
|
|
XM_011514298.1:c.4067C>G
|
XP_011512600.1:p.Thr1356Ser
|
|
XM_011514299.1:c.4199C>G
|
XP_011512601.1:p.Thr1400Ser
|
|
XM_011514300.1:c.4019C>G
|
XP_011512602.1:p.Thr1340Ser
|
|
XM_011514301.1:c.3956C>G
|
XP_011512603.1:p.Thr1319Ser
|
|
XM_011514302.1:c.3800C>G
|
XP_011512604.1:p.Thr1267Ser
|
|
XM_011514299.2:c.4199C>G
|
XP_011512601.1:p.Thr1400Ser
|
|
XM_011514300.2:c.4019C>G
|
XP_011512602.1:p.Thr1340Ser
|
|
XM_011514302.2:c.3800C>G
|
XP_011512604.1:p.Thr1267Ser
|
|
XM_017010250.1:c.4913C>G
|
XP_016865739.1:p.Thr1638Ser
|
|
XM_017010251.2:c.3731C>G
|
XP_016865740.1:p.Thr1244Ser
|
|
NM_080680.3:c.4913C>G
MANE Select
|
NP_542411.2:p.Thr1638Ser
|
|
NM_080681.3:c.4655C>G
|
NP_542412.2:p.Thr1552Ser
|
|
NM_080679.3:c.4592C>G
|
NP_542410.2:p.Thr1531Ser
|
|