ENST00000383408.7:c.3178T>C
|
ENSP00000372900.4:p.Tyr1060His
|
|
ENST00000686869.1:n.3235T>C
|
|
|
ENST00000674853.1:c.3178T>C
MANE Select
|
ENSP00000501957.1:p.Tyr1060His
|
|
ENST00000302079.10:c.3103T>C
|
ENSP00000303316.6:p.Tyr1035His
|
|
ENST00000383408.6:c.2956T>C
|
ENSP00000372900.3:p.Tyr986His
|
|
ENST00000503781.7:c.3103T>C
|
ENSP00000421377.3:p.Tyr1035His
|
|
ENST00000580640.5:c.3178T>C
|
ENSP00000463094.1:p.Tyr1060His
|
|
ENST00000582913.5:c.3145T>C
|
ENSP00000462115.1:p.Tyr1049His
|
|
NM_022068.3:c.3103T>C
|
NP_071351.2:p.Tyr1035His
|
|
XM_011525723.1:c.3235T>C
|
XP_011524025.1:p.Tyr1079His
|
|
XM_011525724.1:c.3178T>C
|
XP_011524026.1:p.Tyr1060His
|
|
XM_011525725.1:c.3145T>C
|
XP_011524027.1:p.Tyr1049His
|
|
XM_011525726.1:c.3235T>C
|
XP_011524028.1:p.Tyr1079His
|
|
XM_011525727.1:c.3235T>C
|
XP_011524029.1:p.Tyr1079His
|
|
XM_011525723.3:c.3235T>C
|
XP_011524025.1:p.Tyr1079His
|
|
XM_011525724.3:c.3178T>C
|
XP_011524026.1:p.Tyr1060His
|
|
XM_011525725.3:c.3145T>C
|
XP_011524027.1:p.Tyr1049His
|
|
XM_011525726.3:c.3235T>C
|
XP_011524028.1:p.Tyr1079His
|
|
XM_017025918.2:c.3196T>C
|
XP_016881407.1:p.Tyr1066His
|
|
XR_001753259.2:n.4232T>C
|
|
|
NM_001378183.1:c.3178T>C
MANE Select
|
NP_001365112.1:p.Tyr1060His
|
|
NM_022068.4:c.3103T>C
|
NP_071351.2:p.Tyr1035His
|
|