ENST00000452035.7:n.2115T>C
|
|
|
ENST00000483004.2:c.1507T>C
|
ENSP00000419887.2:p.Tyr503His
|
|
ENST00000698628.1:c.1624+314T>C
|
ENSP00000513848.1:n.1624+314T>C
|
|
ENST00000698629.1:n.1900T>C
|
|
|
ENST00000698630.1:n.2439T>C
|
|
|
ENST00000698631.1:n.2440T>C
|
|
|
ENST00000698632.1:n.3234T>C
|
|
|
ENST00000698633.1:n.3124T>C
|
|
|
ENST00000698636.1:n.1945T>C
|
|
|
ENST00000425368.7:c.1723T>C
MANE Select
|
ENSP00000416561.2:p.Tyr575His
|
|
ENST00000425368.6:c.1723T>C
|
ENSP00000416561.2:p.Tyr575His
|
|
ENST00000456570.5:c.3229T>C
|
ENSP00000410815.1:p.Tyr1077His
|
|
ENST00000467360.1:n.849T>C
|
|
|
ENST00000477310.1:c.2776T>C
|
ENSP00000418996.1:p.Tyr926His
|
|
ENST00000483004.1:c.345T>C
|
|
|
NM_001710.5:c.1723T>C , LRG_136t1:c.1723T>C
|
NP_001701.2:p.Tyr575His
|
|
NM_001710.6:c.1723T>C
MANE Select
|
NP_001701.2:p.Tyr575His
|
|