ENST00000624552.4:c.14896T>C
|
ENSP00000485357.2:p.Tyr4966His
|
|
ENST00000683500.2:c.14953T>C
MANE Select
|
ENSP00000508292.2:p.Tyr4985His
|
|
ENST00000623487.1:n.3299T>C
|
|
|
ENST00000624552.3:c.14893T>C
|
ENSP00000485357.1:p.Tyr4965His
|
|
NM_001291815.1:c.14953T>C
|
NP_001278744.1:p.Tyr4985His
|
|
XM_011518465.1:c.14830T>C
|
XP_011516767.1:p.Tyr4944His
|
|
XM_011518466.1:c.14821T>C
|
XP_011516768.1:p.Tyr4941His
|
|
XM_011518467.1:c.14776T>C
|
XP_011516769.1:p.Tyr4926His
|
|
NM_001291815.2:c.14953T>C
MANE Select
|
NP_001278744.1:p.Tyr4985His
|
|
XM_011518465.2:c.14830T>C
|
XP_011516767.1:p.Tyr4944His
|
|
XM_011518466.2:c.14821T>C
|
XP_011516768.1:p.Tyr4941His
|
|
XM_011518467.2:c.14776T>C
|
XP_011516769.1:p.Tyr4926His
|
|
XM_017014585.1:c.11734T>C
|
XP_016870074.1:p.Tyr3912His
|
|
XM_017014586.1:c.7531T>C
|
XP_016870075.1:p.Tyr2511His
|
|
XR_001746957.1:n.92+215A>G
|
|
|
XR_001746958.1:n.92+215A>G
|
|
|