ENST00000260197.12:c.4762T>C
MANE Select
|
ENSP00000260197.6:p.Tyr1588His
|
|
ENST00000260197.11:c.4762T>C
|
ENSP00000260197.6:p.Tyr1588His
|
|
ENST00000525532.5:c.1594T>C
|
ENSP00000434634.1:p.Tyr532His
|
|
ENST00000527934.1:c.607T>C
|
ENSP00000435405.1:p.Tyr203His
|
|
ENST00000532694.5:c.1300T>C
|
ENSP00000432131.1:p.Tyr434His
|
|
ENST00000534286.5:c.1492T>C
|
ENSP00000436447.1:p.Tyr498His
|
|
NM_003105.5:c.4762T>C
|
NP_003096.1:p.Tyr1588His
|
|
XM_011542963.1:c.4648T>C
|
XP_011541265.1:p.Tyr1550His
|
|
XM_011542964.1:c.4762T>C
|
XP_011541266.1:p.Tyr1588His
|
|
XM_011542965.1:c.3223T>C
|
XP_011541267.1:p.Tyr1075His
|
|
XM_011542966.1:c.2122T>C
|
XP_011541268.1:p.Tyr708His
|
|
XM_011542967.1:c.1594T>C
|
XP_011541269.1:p.Tyr532His
|
|
XM_011542963.3:c.4648T>C
|
XP_011541265.1:p.Tyr1550His
|
|
XM_011542965.3:c.3223T>C
|
XP_011541267.1:p.Tyr1075His
|
|
XM_011542967.3:c.1594T>C
|
XP_011541269.1:p.Tyr532His
|
|
XM_017018169.2:c.4450T>C
|
XP_016873658.1:p.Tyr1484His
|
|
XM_017018170.2:c.4237T>C
|
XP_016873659.1:p.Tyr1413His
|
|
XM_017018171.1:c.4762T>C
|
XP_016873660.1:p.Tyr1588His
|
|
XM_017018172.2:c.2122T>C
|
XP_016873661.1:p.Tyr708His
|
|
NM_003105.6:c.4762T>C
MANE Select
|
NP_003096.2:p.Tyr1588His
|
|