ENST00000710359.1:c.7000C>G
|
ENSP00000518230.1:p.Pro2334Ala
|
|
ENST00000379802.8:c.8329C>G
MANE Select
|
ENSP00000369129.3:p.Pro2777Ala
|
|
ENST00000379802.7:c.8329C>G
|
ENSP00000369129.3:p.Pro2777Ala
|
|
ENST00000418664.2:c.6532C>G
|
ENSP00000396591.2:p.Pro2178Ala
|
|
NM_001008844.1:c.6532C>G
|
NP_001008844.1:p.Pro2178Ala
|
|
NM_004415.2:c.8329C>G , LRG_423t1:c.8329C>G
|
NP_004406.2:p.Pro2777Ala
|
|
XM_011514323.1:c.7000C>G
|
XP_011512625.1:p.Pro2334Ala
|
|
NM_001008844.2:c.6532C>G
|
NP_001008844.1:p.Pro2178Ala
|
|
NM_001319034.1:c.7000C>G
|
NP_001305963.1:p.Pro2334Ala
|
|
NM_004415.3:c.8329C>G
|
NP_004406.2:p.Pro2777Ala
|
|
NM_004415.4:c.8329C>G
MANE Select
|
NP_004406.2:p.Pro2777Ala
|
|
NM_001008844.3:c.6532C>G
|
NP_001008844.1:p.Pro2178Ala
|
|
NM_001319034.2:c.7000C>G
|
NP_001305963.1:p.Pro2334Ala
|
|