ENST00000557334.6:c.130T>C
|
ENSP00000452512.1:p.Tyr44His
|
|
ENST00000685328.1:c.469T>C
|
ENSP00000508921.1:p.Tyr157His
|
|
ENST00000686877.1:c.*440T>C
|
ENSP00000510431.1:n.*440T>C
|
|
ENST00000687356.1:c.*167T>C
|
ENSP00000510511.1:n.*167T>C
|
|
ENST00000688228.1:n.943T>C
|
|
|
ENST00000688940.1:c.469T>C
|
ENSP00000509238.1:p.Tyr157His
|
|
ENST00000690406.1:c.272T>C
|
|
|
ENST00000690804.1:c.*430T>C
|
ENSP00000508568.1:n.*430T>C
|
|
ENST00000692768.1:c.271T>C
|
ENSP00000510254.1:p.Tyr91His
|
|
ENST00000693229.1:c.394T>C
|
ENSP00000509223.1:p.Tyr132His
|
|
ENST00000256078.10:c.*23T>C
MANE Plus Clinical
|
ENSP00000256078.5:n.*23T>C
|
|
ENST00000311936.8:c.469T>C
MANE Select
|
ENSP00000308495.3:p.Tyr157His
|
|
ENST00000256078.8:c.*23T>C
|
ENSP00000256078.4:n.*23T>C
|
|
ENST00000311936.7:c.469T>C
|
ENSP00000308495.3:p.Tyr157His
|
|
ENST00000557334.5:c.130T>C
|
ENSP00000452512.1:p.Tyr44His
|
|
NM_004985.4:c.469T>C
|
NP_004976.2:p.Tyr157His
|
|
NM_033360.3:c.*23T>C
|
NP_203524.1:n.*23T>C
|
|
XM_006719069.2:c.*23T>C
|
XP_006719132.1:n.*23T>C
|
|
XM_011520653.1:c.469T>C
|
XP_011518955.1:p.Tyr157His
|
|
XM_006719069.4:c.*23T>C
|
XP_006719132.1:n.*23T>C
|
|
XM_011520653.3:c.469T>C
|
XP_011518955.1:p.Tyr157His
|
|
NM_001369786.1:c.*23T>C
|
NP_001356715.1:n.*23T>C
|
|
NM_001369787.1:c.469T>C
|
NP_001356716.1:p.Tyr157His
|
|
NM_004985.5:c.469T>C
MANE Select
|
NP_004976.2:p.Tyr157His
|
|
NM_033360.4:c.*23T>C
MANE Plus Clinical
|
NP_203524.1:n.*23T>C
|
|