ENST00000296782.10:c.2515T>C
|
ENSP00000296782.5:p.Tyr839His
|
|
ENST00000503698.2:c.475T>C
|
ENSP00000518563.1:p.Tyr159His
|
|
ENST00000514735.2:c.2467T>C
|
ENSP00000423162.2:p.Tyr823His
|
|
ENST00000711063.1:c.2515T>C
|
ENSP00000518562.1:p.Tyr839His
|
|
ENST00000357387.8:c.2515T>C
MANE Select
|
ENSP00000349959.3:p.Tyr839His
|
|
ENST00000296782.9:c.2515T>C
|
ENSP00000296782.5:p.Tyr839His
|
|
ENST00000357387.7:c.2515T>C
|
ENSP00000349959.3:p.Tyr839His
|
|
ENST00000503698.1:n.475T>C
|
|
|
ENST00000511516.5:c.*1739T>C
|
ENSP00000423019.1:n.*1739T>C
|
|
NM_001285439.1:c.2515T>C
|
NP_001272368.1:p.Tyr839His
|
|
NM_001285440.1:c.1660T>C
|
NP_001272369.1:p.Tyr554His
|
|
NM_152756.4:c.2515T>C
|
NP_689969.2:p.Tyr839His
|
|
XM_006714463.2:c.2515T>C
|
XP_006714526.1:p.Tyr839His
|
|
XM_011514005.1:c.2515T>C
|
XP_011512307.1:p.Tyr839His
|
|
XM_011514006.1:c.2326T>C
|
XP_011512308.1:p.Tyr776His
|
|
XM_011514007.1:c.1660T>C
|
XP_011512309.1:p.Tyr554His
|
|
XM_006714463.3:c.2515T>C
|
XP_006714526.1:p.Tyr839His
|
|
XM_011514005.2:c.2515T>C
|
XP_011512307.1:p.Tyr839His
|
|
XM_011514006.3:c.2326T>C
|
XP_011512308.1:p.Tyr776His
|
|
XM_017009311.1:c.2467T>C
|
XP_016864800.1:p.Tyr823His
|
|
XM_017009312.1:c.2467T>C
|
XP_016864801.1:p.Tyr823His
|
|
XM_017009313.1:c.2356T>C
|
XP_016864802.1:p.Tyr786His
|
|
XM_017009314.2:c.1660T>C
|
XP_016864803.1:p.Tyr554His
|
|
XM_017009315.2:c.1660T>C
|
XP_016864804.1:p.Tyr554His
|
|
NM_152756.5:c.2515T>C
MANE Select
|
NP_689969.2:p.Tyr839His
|
|
NM_001285439.2:c.2515T>C
|
NP_001272368.1:p.Tyr839His
|
|
NM_001285440.2:c.1660T>C
|
NP_001272369.1:p.Tyr554His
|
|