ENST00000375076.9:c.966A>C
MANE Select
|
ENSP00000364217.4:p.Glu322Asp
|
|
ENST00000375055.6:c.966A>C
|
ENSP00000364195.2:p.Glu322Asp
|
|
ENST00000375065.6:c.153A>C
|
ENSP00000364206.6:p.Glu51Asp
|
|
ENST00000375067.7:c.811A>C
|
ENSP00000364208.3:p.Thr271Pro
|
|
ENST00000375069.7:c.1014A>C
|
ENSP00000364210.4:p.Glu338Asp
|
|
ENST00000375070.7:c.662-154A>C
|
ENSP00000364211.4:n.662-154A>C
|
|
ENST00000375076.8:c.966A>C
|
ENSP00000364217.4:p.Glu322Asp
|
|
ENST00000438221.6:c.1014A>C
|
ENSP00000387887.2:p.Glu338Asp
|
|
ENST00000469940.5:n.5A>C
|
|
|
ENST00000473619.5:n.508A>C
|
|
|
ENST00000484849.5:n.1173A>C
|
|
|
ENST00000488669.5:n.508A>C
|
|
|
ENST00000620802.4:c.283-198A>C
|
ENSP00000484081.1:n.283-198A>C
|
|
NM_001136.4:c.966A>C
|
NP_001127.1:p.Glu322Asp
|
|
NM_001206929.1:c.1014A>C
|
NP_001193858.1:p.Glu338Asp
|
|
NM_001206932.1:c.924A>C
|
NP_001193861.1:p.Glu308Asp
|
|
NM_001206934.1:c.1014A>C
|
NP_001193863.1:p.Glu338Asp
|
|
NM_001206936.1:c.914A>C
|
NP_001193865.1:p.Asn305Thr
|
|
NM_001206940.1:c.966A>C
|
NP_001193869.1:p.Glu322Asp
|
|
NM_001206954.1:c.824A>C
|
NP_001193883.1:p.Asn275Thr
|
|
NM_001206966.1:c.966A>C
|
NP_001193895.1:p.Glu322Asp
|
|
NM_172197.2:c.811A>C
|
NP_751947.1:p.Thr271Pro
|
|
NR_038190.1:n.1249A>C
|
|
|
XM_017010328.2:c.965A>C
|
XP_016865817.1:p.Asn322Thr
|
|
XR_001743189.2:n.1030A>C
|
|
|
XR_001743190.2:n.982A>C
|
|
|
NM_001136.5:c.966A>C
MANE Select
|
NP_001127.1:p.Glu322Asp
|
|
NM_001206932.2:c.924A>C
|
NP_001193861.1:p.Glu308Asp
|
|
NM_001206936.2:c.914A>C
|
NP_001193865.1:p.Asn305Thr
|
|
NM_001206940.2:c.966A>C
|
NP_001193869.1:p.Glu322Asp
|
|
NM_001206954.2:c.824A>C
|
NP_001193883.1:p.Asn275Thr
|
|
NM_001206966.2:c.966A>C
|
NP_001193895.1:p.Glu322Asp
|
|
NM_172197.3:c.811A>C
|
NP_751947.1:p.Thr271Pro
|
|
NR_038190.2:n.1180A>C
|
|
|
NM_001206929.2:c.1014A>C
|
NP_001193858.1:p.Glu338Asp
|
|
NM_001206934.2:c.1014A>C
|
NP_001193863.1:p.Glu338Asp
|
|