ENST00000710359.1:c.4476T=
|
ENSP00000518230.1:p.Tyr1492=
|
|
ENST00000379802.8:c.5805T=
MANE Select
|
ENSP00000369129.3:p.Tyr1935=
|
|
ENST00000379802.7:c.5805T=
|
ENSP00000369129.3:p.Tyr1935=
|
|
ENST00000418664.2:c.4008T=
|
ENSP00000396591.2:p.Tyr1336=
|
|
NM_001008844.1:c.4008T=
|
NP_001008844.1:p.Tyr1336=
|
|
NM_004415.2:c.5805T= , LRG_423t1:c.5805T=
|
NP_004406.2:p.Tyr1935=
|
|
XM_011514323.1:c.4476T=
|
XP_011512625.1:p.Tyr1492=
|
|
NM_001008844.2:c.4008T=
|
NP_001008844.1:p.Tyr1336=
|
|
NM_001319034.1:c.4476T=
|
NP_001305963.1:p.Tyr1492=
|
|
NM_004415.3:c.5805T=
|
NP_004406.2:p.Tyr1935=
|
|
NM_004415.4:c.5805T=
MANE Select
|
NP_004406.2:p.Tyr1935=
|
|
NM_001008844.3:c.4008T=
|
NP_001008844.1:p.Tyr1336=
|
|
NM_001319034.2:c.4476T=
|
NP_001305963.1:p.Tyr1492=
|
|